| TFAP2A |
AP-2 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFAP2B |
AP-2 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFAP2C |
AP-2 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFAP2D |
AP-2 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds the same GCCTGAGGC sequence as the other AP-2s (PMID: 24789576) |
| TFAP2E |
AP-2 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARID1A |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Non-specific DNA binder (PMID: 15170388). |
| ARID1B |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Non-specific DNA binder (PMID: 15170388). |
| ARID3A |
ARID/BRIGHT |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ARID3B |
ARID/BRIGHT |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARID3C |
ARID/BRIGHT |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARID4A |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
Binds DNA in a sequence non-specific manner (PMID: 15640446). |
| ARID4B |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in a sequence non-specific manner (PMID: 15640446). |
| ARID5A |
ARID/BRIGHT |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ARID5B |
ARID/BRIGHT |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
Has a putative AT-hook |
|
| JARID2 |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Only ARID3 and ARID5 family members have sequence specificity (PMID: 15640446). |
| KDM5A |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| KDM5B |
ARID/BRIGHT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds GC-rich sequences such as CCGCCC (PMID: 18270511). |
| KDM5C |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| KDM5D |
ARID/BRIGHT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Polycomb protein that is well-documented to bind histone marks (PMID: 27477906; PMID: 17351630; PMID: 17320160; PMID: 17320162). |
| ARID2 |
ARID/BRIGHT; RFX |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AHCTF1 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AHDC1 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AKNA |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds AT-rich promoters of CD40 and CD40L and coordinates their expression (PMID: 11268217). |
| ASH1L |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| CBX2 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| DNTTIP1 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| DOT1L |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| GLYR1 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| HMGA1 |
AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| HMGA2 |
AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| PHF20 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PHF21A |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| PRR12 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SCML4 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SETBP1 |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Orthologous protein from mouse (Setbp1) bind DNA sequence-specifically by PBM |
| SRCAP |
AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| C11orf95 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| FAM200B |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SGSM2 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBED1 |
BED ZF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBED2 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a BED domain that should bind DNA, but lacks the dimerization domain (PMID: 20016685). |
| ZBED3 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBED4 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBED5 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBED6 |
BED ZF |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZBED8 |
BED ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Despite its name, does not have a detectable BED ZF domain. |
| ZBED9 |
BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AHR |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| AHRR |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ARNT |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ARNT2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARNTL |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARNTL2 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
High-throughput in vitro |
|
ARNTL2 Forms heterodimers with CLOCK and NPAS2 (PMID:10864977 ). |
| ASCL1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ASCL2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ASCL3 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
High-throughput in vitro |
|
ASCL1 heterodimerizes with TCF3; TCF4 and TCF12 (PMID: 24835951). |
| ASCL4 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Probably heterodimerizes with TCF3; TCF4 or TCF12 like the other ASCL TFs |
| ASCL5 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Probably heterodimerizes with TCF3; TCF4 or TCF12 like the other ASCL TFs |
| ATOH1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATOH7 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATOH8 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BHLHA15 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BHLHA9 |
bHLH |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
Protein heterodimerizes with TCF3; TCF4 and TCF12 (PMID: 25466284). |
| BHLHE22 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BHLHE23 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BHLHE40 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BHLHE41 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CCDC169-SOHLH2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| CLOCK |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Can also bind as heterodimer with ARNTL. |
| EPAS1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| FERD3L |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FIGLA |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HAND1 |
bHLH |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Obligate heteromer (PMID: 10611232). |
| HAND2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HELT |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Can form homodimers or heterodimers with HEY2 and HES5, suggesting also that the HELT homodimer is dependent of a additional Orange domain while the HEY2 heterodimer requires just the DBD (PMID: 14764602). |
| HES1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES3 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES4 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES5 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES6 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HES7 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also forms heterodimers. |
| HEY1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HEY2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HEYL |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HIF1A |
bHLH |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds as obligate heteromer with ARNT (PMID: 9027737). |
| HIF3A |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Binds DNA as a heterodimer with ARNT and ARNT2; reviewed in (PMID: 24099156). |
| ID1 |
bHLH |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ID bHLH proteins lack the basic region and should not be able to bind DNA. The HT-SELEX motif for ID4 is likely by a co-precipitated protein or it is a contamination |
| ID2 |
bHLH |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ID bHLH proteins lack the basic region and should not be able to bind DNA. The HT-SELEX motif for ID4 is likely by a co-precipitated protein or it is a contamination |
| ID3 |
bHLH |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ID bHLH proteins lack the basic region and should not be able to bind DNA. The HT-SELEX motif for ID4 is likely by a co-precipitated protein or it is a contamination |
| ID4 |
bHLH |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ID bHLH proteins lack the basic region and should not be able to bind DNA. The HT-SELEX motif for ID4 is likely by a co-precipitated protein or it is a contamination |
| LYL1 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
TAL1, TAL2 and LYL are very similar and have a basic region with a bulky tryptophan inserting into the cluster of the basic residues. Binds DNA as a heterodimer with TCF3 (PDB:2YPB and PDB:2YPA). |
| MAX |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MESP1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MESP2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MITF |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Binds DNA both as homo- and heterodimers (PMID: 23207919). The structure 4ATI is a homodimer with DNA GTTAGCACATGACCCT. |
| MLX |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MLXIP |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
High-throughput in vitro |
|
|
| MLXIPL |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MNT |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Prefers to heterodimerize with MAX over homodimer formation (PMID: 9000049). |
| MSC |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MSGN1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MXD1 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
All three MXD proteins have very similar sequences and should behave accordingly, making heterodimers with at least MAX (PMID:8521822). |
| MXD3 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
All three MXD proteins have very similar sequences and should behave accordingly, making heterodimers with at least MAX (PMID:8521822). |
| MXD4 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
All three MXD proteins have very similar sequences and should behave accordingly, making heterodimers with at least MAX (PMID:8521822). |
| MXI1 |
bHLH |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Has a putative AT-hook |
Obligate heteromer (PMID: 8425219). |
| MYC |
bHLH |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Functions as a heterodimer with MAX. |
| MYCL |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Similar to MYC and thus likely to functions as a heterodimer with MAX. |
| MYCN |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MYF5 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| MYF6 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MYOD1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MYOG |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NCOA1 |
bHLH |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
NCOA1/2/3 all have been tested on PBMs and HT-SELEX without yielding a motif. All are co-activators, collectively suggesting they might be obligate heteromers. |
| NCOA2 |
bHLH |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
NCOA1/2/3 all have been tested on PBMs and HT-SELEX without yielding a motif. All are co-activators, collectively suggesting they might be obligate heteromers. |
| NCOA3 |
bHLH |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
NCOA1/2/3 all have been tested on PBMs and HT-SELEX without yielding a motif. All are co-activators, collectively suggesting they might be obligate heteromers. |
| NEUROD1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROD2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROD4 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROD6 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROG1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROG2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NEUROG3 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NHLH1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NHLH2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NPAS1 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Likely obligate heteromer (PMID: 27782878). |
| NPAS2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NPAS3 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Likely obligate heteromer (PMID: 9374395; PMID: 27782878). |
| NPAS4 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
High-throughput in vitro |
|
Likely dimerizes with ARNT2 (PMID:24263188). |
| OLIG1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OLIG2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
OLIG2 can homodimerize and heterodimerize with OLIG1 and NGN2 (PMID:15655114; PMID: 21382552). |
| OLIG3 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PTF1A |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SCX |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
SCX heterodimerizes with TCF3 (PMID: 19828133). The Taipale lab has an unpublished HT-SELEX model; both it and the inferred B1H motif seem very weak, supporting the idea that the homodimer does not bind DNA well. |
| SIM1 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Similar to SIM2, which is a likely obligate heteromer. |
| SIM2 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Likely obligate hetereomer (PMID: 7592839) |
| SOHLH1 |
bHLH |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
Forms SOHLH1-SOHLH2 heterodimers (PMID: 22056784). |
| SOHLH2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SREBF1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SREBF2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TAL1 |
bHLH |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
No motif yielded from PBMs or HT-SELEX. Binds DNA as heterodimer with TCF3 (PDB:2YPB and PDB:2YPA). |
| TAL2 |
bHLH |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
No motif yielded from PBMs or HT-SELEX. Similar to TAL1, which binds DNA as heterodimer with TCF3 (PDB:2YPB and PDB:2YPA). |
| TCF12 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF15 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF21 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF23 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Basic region is very similar to TCF21, which binds DNA as a homodimer in HT-SELEX. |
| TCF24 |
bHLH |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF3 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF4 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCFL5 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFAP4 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also can form heterodimers (PMID: 26550823). |
| TFE3 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFEB |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFEC |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TWIST1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Can form both homodimers and heterodimers with TCF3 (PMID: 16502419). |
| TWIST2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| USF1 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| USF2 |
bHLH |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| USF3 |
bHLH |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| POGK |
Brinker |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AC023509.3 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Identical bZIP DBD to ATF7. Some isoforms also contain a single C2H2 ZF. This is known to facilitate protein interactions in ATF7 (see ATF7 Uniprot page), so AC023509.3 is only classified here as a bZIP protein |
| APC2 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| ATF1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ATF2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATF3 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATF4 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATF5 |
bZIP |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Transfac motifs dont correspond to canonical bZIP binding sites. Annotated as obligate heteromer based on peptide array studies (PMID:12805554). |
| ATF6 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATF6B |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ATF7 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Some isoforms also contain a single C2H2 ZF. This is known to facilitate protein interactions (see Uniprot page), so ATF7 is only classified here as a bZIP protein |
| BACH1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| BACH2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Based on Newman et al 2003 (PMID: 12805554), the protein has strong preference for forming heterodimers with MAFG and MAFK over homo-dimerisation. The Homer ChIP-seq motif appears to be a MAF-BACH2 heterodimer. |
| BATF |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Prefers to heterodimerize, but it has an HT-SELEX (homodimer) motif. Its homodimerization Kd is 184nM and its best heterodimer is with CEBPG (<1nM) (PMID: 23661758). |
| BATF2 |
bZIP |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
Part of AP-1 complex - there is no evidence it can bind on its own as a homodimer. |
| BATF3 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Transfac motif is dubious. |
| BEND4 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lacks the basic region of the bZIP domain. |
| CCDC3 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
bZIP domain is truncated and lacks the DNA-contacting residues. |
| CCDC83 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
bZIP domains are truncated, such that they are likely just coiled-coiled regions with no DNA-binding ability. |
| CEBPA |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| CEBPB |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CEBPD |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
CEBPD binds as both a homodimer and as a heterdimer with other C/EBP TFs (PMID: 1884998; PMID: 12805554). |
| CEBPE |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also forms heterodimers. |
| CEBPG |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREB1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREB3 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREB3L1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREB3L2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| CREB3L3 |
bZIP |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Gel-shift and reporter experiments demonstrate that CREB3L3 is a TF (PMID: 11353085). |
| CREB3L4 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREB5 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREBL2 |
bZIP |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREBRF |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Tested on HT-SELEX and did not yield a motif. Binds to CREB3 and represses the unfolded protein response (PMID: 18391022). |
| CREBZF |
bZIP |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CREM |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DBP |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DDIT3 |
bZIP |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Has strong preference for forming heterodimers with BATF; DBP; HLF; CEBP[ABCD] over homodimerization (PMID: 12805554). |
| FOS |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOSB |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOSL1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOSL2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also forms heterodimers. |
| GULP1 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| HLF |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOOK2 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| IQGAP1 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
bZIP domain in the protein is just a fragment. |
| JDP2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| JUN |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| JUNB |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Prefers forming heterodimers with FOS; FOSB; FOSL1 and FOSL2 over homodimers (PMID:12805554); but, clearly can bind DNA specifically in vitro. |
| JUND |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KIF15 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Has a bZIP like fragment that lacks the basic region required for DNA binding and a STE-domain that is classified as a potential DBD in CIS-BP. It is a kinesin operating in the microtubule system (PMID: 24419385) |
| KRT13 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| MAF |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MAFA |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MAFB |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
PDB:2WTY is a homodimer crystallised with TAATTGCTGACTCAGCAAAT sequence |
| MAFF |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MAFG |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MAFK |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MORC3 |
bZIP |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Lacks a canonical bZIP DBD but: regulates TP53 activity (PMID: 17332504]), binds RNA in vitro (PMID: 11927593), and may be required for influenza A transcription during viral infection (PMID: 26202233). |
| NDC80 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| NFE2 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFE2L1 |
bZIP |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Tested on HT-SELEX and PBM. Neither yielded a motif. Likely an obligate heteromer (PMID: 23661758). |
| NFE2L2 |
bZIP |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Has been tested by both PBM and HT-SELEX. Neither yielded a motif. Likely obligate heteromer. |
| NFE2L3 |
bZIP |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Tested on HT-SELEX and PBM. Neither yielded a motif. Likely an obligate heteromer (PMID: 23661758). Strong preference for forming heterodimers with MAFG and MAFK over homodimers (PMID: 12805554). |
| NFIL3 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NRBF2 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignments, the protein is only weakly related to the other bZIP proteins and lacks the basic region required for DNA binding |
| NRL |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PPP1R21 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein lacks the basic region these proteins use to contact the DNA |
| RAB11FIP4 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely false-positive - appears to function primarily in the cytoplasm (PMID: 12470645). |
| RNF219 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Not a proper bZIP; contains only a small leucine zipper region but lacks the DNA-interfacing basic part. |
| SCOC |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Not a proper bZIP; contains only a small leucine zipper region but lacks the DNA-interfacing basic part. |
| TEF |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TRAK2 |
bZIP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The bZIP domain is only a partial 40AA sequence that will not bind DNA. |
| XBP1 |
bZIP |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| AC008770.3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AC092835.1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
KRAB C2H2 Protein |
| AC138696.1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| AEBP2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| AKAP8 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
(PMID: 26683827) uses SELEX to show binding to G/C rich DNA, and confirms association with rDNA promoters. Also claims it has a C2H2 domain. Interpro says it has a C2H2 AKAP95-type 1 and a C2H2 AKAP95-type 2 domain. SMART does identify a single C2H2 domain. |
| AKAP8L |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
This is homologous to the AKAP8/AKAP95 protein. which has been shown by SELEX to bind GC rich sequences (PMID: 26683827). |
| ANKZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ATMIN |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| BCL11A |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| BCL11B |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BCL6 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BCL6B |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BNC1 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| BNC2 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Has a putative AT-hook |
|
| CASZ1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| CCDC17 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| CHAMP1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| CPXCR1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| CTCF |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| CTCFL |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| DPF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
This protein contains C2H2 ZFs missed by Pfam scanning. |
| DPF3 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Single C2H2 domain |
Single C2H2 ZF. PHD domains mediate recognition of acetylated histones (PMID: 20613843); unclear if the ZF contributes DNA-binding specificity to the interaction. |
| DZIP1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain; Has a putative AT-hook |
|
| E4F1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| EEA1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Based on (PMID: 20534488), the protein has a C2H2 ZF domain; but it uses the domain for contacting RAB5A rather than for binding DNA. |
| EGR1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EGR2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Binds HOX4A promoter (PMID:21836637) |
| EGR3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EGR4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FAM170A |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Degenerate C2H2-ZFP. Localizes to the nucleus and overexpression upregulates other genes (PMID: 20162441). |
| FEZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| FEZF2 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FIZ1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Protein has a decent cassette of C2H2 ZF domains (not all are detected by Pfam). It has been also shown to interact with homeodomain protein CRX (PMID: 18854042) and MAF-subtype bZIP protein NRL (PMID: 12566383). |
| GFI1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GFI1B |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GLI1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| GLI2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GLI3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GLI4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
Protein is not closely homologous to GLI1-3 proteins. |
| GLIS1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GLIS2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GLIS3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GTF3A |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| GZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| HIC1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HIC2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HINFP |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HIVEP1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| HIVEP2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| HIVEP3 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Has a putative AT-hook |
Binds to NFKB-like consensus sequence to repress transcription (PMID: 21189157). PWMs for HIVEP1 and 2 in Transfac and Hocomoco are also NFKB-like. |
| HKR1 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| IKZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| IKZF2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| IKZF3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| IKZF4 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| IKZF5 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| INSM1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| INSM2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| JAZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| KAT7 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| KCMF1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
No evidence of DNA-binding in the literature; and has evidence of E3 ligase activity (PMID:15581609). |
| KIN |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Binds curved DNA (PMID: 8078469). |
| KLF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF10 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF11 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF12 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF13 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF14 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF15 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF16 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF17 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF5 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Binds as a monomer and as a dimer (PMID: 25575120). |
| KLF6 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| KLF7 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| KLF8 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| KLF9 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| L3MBTL1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Histone modifier; polycomb protein. |
| L3MBTL3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Histone modifier; polycomb protein. |
| L3MBTL4 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Histone modifier; polycomb protein. |
| MAZ |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| MECOM |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| MTF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MYNN |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| MYT1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Crystal structure (PDB:2JX1) has GTGAACTTTCGGT DNA; similar to MYT1L SELEX and PBM sites. |
| MYT1L |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| NUFIP1 |
C2H2 ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
Single C2H2 domain |
This is a known RNA-binding protein with a single C2H2 domain. TF-CAT considered it a candidate TF; but in the ten years since; no such evidence has emerged. |
| OSR1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OSR2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OVOL1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OVOL2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OVOL3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PEG3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
SCAN C2H2 ZF Protein. |
| PLAG1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PLAGL1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| PLAGL2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PRDM1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PRDM10 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| PRDM12 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| PRDM13 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PRDM14 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| PRDM15 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| PRDM16 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| PRDM2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has been suggested to function as a histone methyltransferase (PMID: 15282304), but it has a decent set of C2H2 ZF domains and could thus bind DNA independently. |
| PRDM4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PRDM5 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of C2H2 ZF domains. Moreover, (PMID: 17636019) has performed SELEX for it and validated the result. |
| PRDM6 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| PRDM8 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PRDM9 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| PRMT3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Has a single C2H2 ZF (PMID: 10931850). |
| RBAK |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| RBSN |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Potential false positive - protein functions in membrane trafficking. |
| REPIN1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds DNA specifically based on EMSA and nuclease footprinting (PMID: 10606657). |
| REST |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| RLF |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| RREB1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| SALL1 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| SALL2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| SALL3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SALL4 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| SCRT1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SCRT2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SLC2A4RG |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Two papers demonstrate a bit of evidence for DNA binding (PMID:10825161 and PMID: 14625278 ). |
| SNAI1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SNAI2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SNAI3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP5 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Transfac motif has some similarity to known Sp1 TF motifs from multiple species and sources |
| SP6 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP7 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| SP8 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP9 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ST18 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TRAFD1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Possible false positive: the protein negatively regulates IRF3 and NFKB but there is no evidence for DNA-binding and it is likely to operate upstream on the signalling cascade (PMID:18849341). |
| TSHZ1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| TSHZ2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Also contains an atypical homodomain (Uniprot) not identified by Pfam. |
| TSHZ3 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
The C2H2 domains are too spread out to be credible; but there is also a homodomain. Seems more likely than not that it binds DNA. |
| VEZF1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| WIZ |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Regulates the G9aGLP complex for gene repression; has a ChIP-seq derived DNA-binding motif (PMID:25789554). |
| WT1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Crystal structure (PDB:2JP9) is with dsDNA GCGCAGACGCCCCCGCG, which is consistent with the PWMs |
| YY1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| YY2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ZBTB10 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a BTB homodimerization domain |
| ZBTB11 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZBTB12 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB14 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB16 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZBTB17 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBTB18 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB20 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB21 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a BTB homodimerization domain |
| ZBTB22 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB25 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBTB26 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ZBTB32 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB33 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZBTB34 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB37 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB38 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
It has a decent cassette of znfC2H2 domains and a BTB homodimerization domain. Requires CpG methylation for binding into a site in MYOG-promoter (PMID: 21625269). |
| ZBTB39 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBTB4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZBTB40 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a BTB homodimerization domain |
| ZBTB41 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBTB42 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZBTB43 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB44 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB45 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB46 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Specificity is unknown; functions in dendritic cells (PMID: 22615130). |
| ZBTB47 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZBTB48 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZBTB49 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB5 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Binds to GATCGGGCGGGGCGGTTGTATATCA; GATCCGTTAGAGGAAGAAGACTGGGCATGTCTG and GATCCATCAGGAACATGTCCCAACATGTTGAGCTC based on EMSA using recombinant protein (PMID: 19491398). |
| ZBTB6 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZBTB7A |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB7B |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB7C |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZBTB8A |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a two znfC2H2 domains and a BTB-domain |
| ZBTB8B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a BTB homodimerization domain |
| ZBTB9 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has two znfC2H2 domains and a BTB-domain that typically mediates homotypic dimerization |
| ZFAT |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| ZFP1 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFP14 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP2 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZFP28 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE); Has a putative AT-hook |
|
| ZFP3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP30 |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFP37 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZFP41 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFP42 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFP57 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
Recognizes CpG methylated ACTGCGGCAAT site based on structure 4GZN |
| ZFP62 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZFP64 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZFP69 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP69B |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP82 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP90 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZFP91 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Possible false positive. An Atypical E3 ubiquitin-protein ligase that mediates Lys-63-linked ubiquitination of MAP3K14/NIK; leading to stabilization and activation of MAP3K14/NIK. It thereby acts as an activator of the non-canonical NF-kappa-B2/NFKB2 pathway (PMID: 20682767). |
| ZFP92 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZFPL1 |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a Golgi apparatus integral membrane protein with RING-type zinc fingers (PMID:18323775 ). |
| ZFPM1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZFPM2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
FOG-proteins use some of their zinc-fingers to interact with the GATA proteins. Other C2H2 ZFs are probably also capable of binding DNA (PMID: 10329627). |
| ZFR |
C2H2 ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZFR2 |
C2H2 ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
ZFR2 contains only RNA-binding zinc fingers |
| ZFX |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZFY |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZIC1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZIC2 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ZIC3 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZIC4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZIC5 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZIK1 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZIM2 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
Binds GKGGSWST consensus with GTGGCAGT as the optimal site based on competition EMSA (PMID: 26692216). |
| ZIM3 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZKSCAN1 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZKSCAN2 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZKSCAN3 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZKSCAN4 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZKSCAN5 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZKSCAN7 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZKSCAN8 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZMAT1 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Possible RBP. |
| ZMAT3 |
C2H2 ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein binds RNA (PMID: 19805223 and PMID: 16844115). |
| ZMAT4 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Possible RBP. |
| ZNF10 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF100 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF101 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF106 |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
C2H2 ZFs are not present in most isoforms; of which most contain WD40 repeats. Previous annotations (TFCat) suggest role as a cofactor (PMID: 15833274). |
| ZNF107 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF112 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains and a KRAB-domain; virtually nothing is known about it. |
| ZNF114 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF117 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF12 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF121 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF124 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF131 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Evidence for DNA binding (PMID: 20303951 ). |
| ZNF132 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF133 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF134 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF135 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF136 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF138 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF14 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF140 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF141 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF142 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF143 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF146 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF148 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF154 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF155 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF157 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF16 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF160 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF165 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a SCAN-domain and that it appears to be expressed commonly in urinary bladder cancers PMID: 25214475 |
| ZNF169 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF17 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF174 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF175 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF177 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF18 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF180 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF181 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF182 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF184 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF189 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF19 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF195 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Kruppel family C2H2 ZF. |
| ZNF197 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF2 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF20 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF200 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF202 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF205 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF207 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF208 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF211 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF212 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF213 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE); Has a putative AT-hook |
|
| ZNF214 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF215 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF217 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Based on (PDB: 3UK3) this protein has at least two DNA binding znf domains. In vitro evidence for DNA binding (PMID:17130829). |
| ZNF219 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds CCCCCA based on SELEX (PMID: 14621294). |
| ZNF22 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF221 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF222 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF223 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF224 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF225 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF226 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF227 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF229 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF23 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF230 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has nice array of znf domains and a KRAB domain |
| ZNF232 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF233 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF234 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF235 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF236 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF239 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds TAAAGGCT based on EMSA (PMID: 11278819). |
| ZNF24 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF248 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF25 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF250 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF251 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF253 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF254 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF256 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF257 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF26 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF260 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF263 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF264 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF266 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF267 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF268 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains znfC2H2 domains and a KRAB-domain; linked to cervical cancer through effects on NFKB-signaling (PMID: 23091055). |
| ZNF273 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF274 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF275 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF276 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF28 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF280A |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF280B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF280C |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF280D |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF281 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF282 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF283 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF284 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF285 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF286A |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF286B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF287 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF292 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF296 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF3 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF30 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF300 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF302 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF304 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF311 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF316 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF317 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF318 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Possible RNA-binding protein; it has two u1 type ZNF domains (PMID: 25057009). |
| ZNF319 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF32 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF320 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF322 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF324 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF324B |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF326 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
ZNF326 is a member of the DBIRD complex that regulates splicing by binding to PolII in an RNA-independant manner (PMID:22446626). |
| ZNF329 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF331 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF333 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF334 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF335 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| ZNF337 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF33A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF33B |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF34 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF341 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF343 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF345 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF346 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds dsDNA with low affinity and no discernible specificity (PMID: 24521053). |
| ZNF347 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF35 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF350 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF354A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF354B |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF354C |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF355P |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
|
| ZNF358 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF362 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF365 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Also contains a Ku C terminal like domain that is thought to be involved in DNA-damage repair pathways. |
| ZNF366 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
This protein has been shown to complex with and function as a corepressor for ESR1 (PMID: 17085477) and glucocorticoid receptor (PMID: 23440419). It has a nice set of znfs and could thus well bind DNA independently. |
| ZNF367 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Virtually nothing is known for this protein except that it has two znfC2H2 domains next to each other |
| ZNF37A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF382 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF383 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF384 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF385A |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF385B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF385C |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF385D |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF391 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF394 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF395 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Contains a single ZF (string matching on Uniprot) that is not identified using Pfam HMM thresholds. Shown to bind a short DNA sequence (GCCGGCG) by EMSA and DNase I footprinting (PMID:14625278). |
| ZNF396 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF397 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and that it binds on centromeric regions PMID: 18369653 |
| ZNF398 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF404 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF407 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Protein has a decent cassette of znfC2H2 domains; a study links it in regulation of glucose intake receptor GLUT4 (PMID: 25596527). |
| ZNF408 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF41 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF410 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF414 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Its on the low end of confidence that its a TF; since most of the domains are variants of C2H2; but its more likely than not since they are in a row. |
| ZNF415 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF416 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF417 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF418 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF419 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF420 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF423 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF425 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF426 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF428 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF429 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF43 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF430 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF431 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF432 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF433 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF436 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF438 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has two znfC2H2 domains and that it represses transcription in a reporter assay PMID: 17669267 |
| ZNF439 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF44 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF440 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF441 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF442 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF443 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF444 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF445 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF446 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains three znfC2H2 domains and represses transcription when expressed as GAL4 fusion (PMID:15936718). |
| ZNF449 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF45 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF451 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF454 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF460 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF461 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Protein has a decent cassette of znfC2H2 domains and a KRAB-domain. It has been shown also to operate as a corepressor of NR5A1, where the KRAB-domain ).mediates both the interaction to NR5A1 and to HDAC2 (PMID: 16595694 |
| ZNF462 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has many znfC2H2 like domains that are however not in tight arrays but interspersed throughout the sequence |
| ZNF467 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF468 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF469 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
|
| ZNF470 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a possible role in chondrocytes (PMID: 15302581). It has a decent cassette of znfC2H2 domains and a KRAB-domain. |
| ZNF471 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF473 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF474 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF479 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF48 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF480 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF483 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF484 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF485 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF486 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF487 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Single C2H2 domain; Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF488 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has two znfC2H2 domains |
| ZNF490 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF491 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF492 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF493 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF496 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF497 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF500 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF501 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF502 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF503 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF506 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
Has a nice cassette of znfC2H2 domains and a KRAB domain |
| ZNF507 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF510 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has decent cassettes of znfC2H2 domains |
| ZNF511 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF512B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Protein has znfC2H2 domains but they are fragmented rather than making decent cassettes |
| ZNF513 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF514 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF516 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF517 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF518A |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and that it interacts with polycomb repressor complex 2 PMID: 25680957 |
| ZNF518B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF519 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF521 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF525 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF526 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF527 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF528 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF529 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF530 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF532 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has decent cassettes of znfC2H2 domains |
| ZNF534 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF536 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF540 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF542P |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
|
| ZNF543 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF544 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF546 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF547 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF548 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF549 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF550 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF551 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF552 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF554 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF555 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF556 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF557 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF558 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF559 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF560 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF561 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF562 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF563 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF564 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF565 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF566 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF567 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF568 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF569 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF57 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains and has been shown to be expressed in many tissues and to be able to repress transcription (PMID: 20356463). |
| ZNF570 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF571 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF572 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF573 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF574 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF575 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF576 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF577 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF578 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF579 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF580 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF581 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF582 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF583 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF584 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF585A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF585B |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF586 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF587 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF587B |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF589 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF592 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF593 |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein has a single atypical znfC2H2 domain that has been shown to inhibit binding of POU2F2 to DNA by interacting with POU2F2 (PMID: 18287285). |
| ZNF594 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF595 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF596 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF597 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF598 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF599 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF600 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF605 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF606 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF607 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF608 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF609 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF610 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF611 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF613 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF614 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF615 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF616 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF618 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF619 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF620 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF621 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF622 |
C2H2 ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
ZNF622 lacks canonical Pfam matches to C2H2 domains and appears to have better homology to U1-type 1 ZFs involved in RNA recognition. Previous evidence for TF activity (PMID:12645566) was based on transcriptional regulation; and not DNA-binding. |
| ZNF623 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF624 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF625 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF626 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF627 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF628 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains. The transfac model doesnt look like a common suspect |
| ZNF629 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF630 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF639 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Promotes transcription of HIV genes (PMID: 24204263). |
| ZNF641 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF644 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Possible false positive. Arrangement of C2H2 domains seems inconsistent with DNA binding. |
| ZNF645 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF646 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF648 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF649 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF652 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF654 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF655 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF658 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF66 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF660 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF662 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF664 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF665 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF667 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF668 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF669 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF670 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains and a KRAB domain |
| ZNF671 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF672 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF674 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF675 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF676 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF677 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF678 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF679 |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF680 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF681 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF682 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF683 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF684 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF687 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF688 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF689 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain and that it downregulates expression of BCL2 proteins in some types of liver cancer PMID: 21624362 |
| ZNF69 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF691 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF692 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF695 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF696 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF697 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF699 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF7 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF70 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF700 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF701 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF703 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF704 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Single C2H2 domain |
|
| ZNF705A |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Contains decent cassette of znfC2H2 domains and a KRAB-domain. |
| ZNF705B |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF705D |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF705E |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains and a KRAB domain |
| ZNF705G |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF706 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF707 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF708 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF709 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF71 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF710 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known about this protein except that it has a nice array of znfC2H2 domains |
| ZNF711 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF713 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF714 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF716 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF717 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF718 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF721 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF724 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain. |
| ZNF726 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF727 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF728 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF729 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF73 |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene; Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Pseudogene |
| ZNF730 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF732 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF735 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF736 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF737 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF74 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF740 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF746 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF747 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF749 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF750 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain; Has a putative AT-hook |
Influences KLF4 expression (PMID: 22364861). |
| ZNF75A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF75D |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF76 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF761 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF763 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF764 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF765 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF766 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF768 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF77 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF770 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF771 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF772 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF773 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF774 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF775 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a MBD domain |
| ZNF776 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF777 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF778 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF780A |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF780B |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF781 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF782 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF783 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF784 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF785 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF786 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF787 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF788 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF789 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF79 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF790 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF791 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF792 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF793 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF799 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF8 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF80 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains. |
| ZNF800 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
C2H2 domains are not arranged in the stereotypic array fashion; but there are several of them. |
| ZNF804A |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF804B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Jaz domain suggests RNA-binding activity |
| ZNF805 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF808 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF81 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF812P |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
|
| ZNF813 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains and a KRAB domain |
| ZNF814 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF816 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF821 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF823 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF827 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has been shown to operate on telomeres and recruit the NuRD complex into them (PMID: 25150861). |
| ZNF829 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF83 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF830 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
Possible false positive. The C2H2 domain is a weak match, and doesnt come up on SMART or PFAM. Mouse ortholog is involved in DNA replication and repair (PMID: 25168238; PMID: 21191184). |
| ZNF831 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF835 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF836 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF837 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a nice cassette of znfC2H2 domains; virtually nothing is known about it otherwise. |
| ZNF839 |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The single C2H2 domain has an insertion between the Hs. Also; it is embedded within the DUF4764 domain; which encompasses most of the protein. Its not located in the usual C2H2 loci. |
| ZNF84 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF841 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF843 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Single C2H2 domain |
|
| ZNF844 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF845 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF846 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZNF85 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF850 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF852 |
C2H2 ZF(KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF853 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains |
| ZNF860 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF865 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF878 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF879 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF880 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF883 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZNF888 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
One transcript is protein-coding |
| ZNF891 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF90 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF91 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF92 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a KRAB-domain |
| ZNF93 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
Kruppel family C2H2 ZF. |
| ZNF98 |
C2H2 ZF(KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZNF99 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZSCAN1 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN10 |
C2H2 ZF(non-KRAB) |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN12 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a SCAN-domain |
| ZSCAN16 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN18 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZSCAN2 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a SCAN-domain |
| ZSCAN20 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZSCAN21 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds AGYACNNNNNNNGGYAC consensus based on SELEX (PMID: 8625807). |
| ZSCAN22 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZSCAN23 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN25 |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a decent cassette of znfC2H2 domains and a SCAN-domain |
| ZSCAN26 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZSCAN29 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| ZSCAN30 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZSCAN31 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
Also known as ZNF323 |
| ZSCAN32 |
C2H2 ZF(KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZSCAN4 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN5A |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZSCAN5B |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZSCAN5C |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
ChIP-seq motif is consistent with recognition code (RCADE) |
|
| ZSCAN5DP |
C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
|
| ZSCAN9 |
C2H2 ZF(non-KRAB) |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZUFSP |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZXDA |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Complexes with CIITA and the similar protein ZXDC to regulate MHCII complex transcription (PMID: 17493635). |
| ZXDB |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZXDC |
C2H2 ZF(non-KRAB) |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PATZ1 |
C2H2 ZF; AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Motif obtained from MEME - not supported by recognition code (RCADE) and may be inaccurate or indirect |
|
| ZBTB24 |
C2H2 ZF; AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZNF524 |
C2H2 ZF; AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZNF653 |
C2H2 ZF; AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZNF277 |
C2H2 ZF; BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has a some znfC2H2 and znfBED domains |
| ZNF512 |
C2H2 ZF; BED ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Virtually nothing is known for this protein except that it has some of znfC2H2 domains and a znfBED domain and could thus be a TF |
| ZEB1 |
C2H2 ZF; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZEB2 |
C2H2 ZF; Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| ZFHX3 |
C2H2 ZF; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFHX4 |
C2H2 ZF; Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Curious protein with numerous C2H2 and homeodomain-like domains. |
| TRERF1 |
C2H2 ZF; Myb/SANT |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Contains a SANT and multiple DNA-binding C2H2 domains. |
| ZNF541 |
C2H2 ZF; Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Has good looking ZF arrays and possible Myb domains. |
| NFYA |
CBF/NF-Y |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Binds as a trimer with NFYB and NFYC. |
| CPSF4 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| CPSF4L |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| DHX57 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| DUS3L |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| HELZ |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| MBNL1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| MBNL2 |
CCCH ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Has methylated and unmethylated HT-SELEX motifs, despite this family largely binding RNA exclusively (PMID: 28473536 ) |
| MBNL3 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| MKRN1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| MKRN2 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| NUPL2 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| PARP12 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely an RNA binding protein (PMID: 25086041). |
| PPP1R10 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Close ortholog (PP1RA) binds to mRNA, single-stranded DNA (ssDNA), poly(A) and poly(G) homopolymers (Uniprot). |
| PRR3 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RC3H1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
A well established RNA-binding protein reviewed in (PMID: 26489670). |
| RC3H2 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RNF113A |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RNF113B |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| TOE1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| TRMT1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| UNK |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| UNKL |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H10 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H11A |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H12A |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H13 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H14 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds UUUNUUU RNA-sequence based on Ray et al 2013 (PMID: 23846655). |
| ZC3H15 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H18 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H3 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H4 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| ZC3H6 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H7A |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H7B |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZC3H8 |
CCCH ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Mouse ortholog can bind DNA specifically, based on EMSA (PMID: 12077251). |
| ZC3HAV1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 22658674; PMID: 22681889). |
| ZFP36 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA binding protein (PMID: 10330172). |
| ZFP36L1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 27102483; PMID: 17013884). |
| ZFP36L2 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 20506496). |
| ZGPAT |
CCCH ZF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds RRRGGAGGAGA based on SELEX and EMSA (PMID: 19644445). |
| ZMAT5 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZRSR1 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| ZRSR2 |
CCCH ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| CENPB |
CENPB |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CENPBD1 |
CENPB |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| JRK |
CENPB |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| JRKL |
CENPB |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TIGD1 |
CENPB |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TIGD2 |
CENPB |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TIGD3 |
CENPB |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| TIGD4 |
CENPB |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Evidence showing that the two HTH domains in the protein together bind specifically to a 17-base-pair sequence; the CENP-B box; which occurs in alpha-satellite DNA in human centromeres (PMID: 16183641). |
| TIGD5 |
CENPB |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| TIGD6 |
CENPB |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TIGD7 |
CENPB |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| CAMTA1 |
CG-1 |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds CGCATTGCG based on EMSA performed in (PMID: 25049392) |
| CAMTA2 |
CG-1 |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| CARHSP1 |
CSD |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 11842224; PMID: 21078874) |
| CSDC2 |
CSD |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 12801884) |
| CSDE1 |
CSD |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Established RNA-binding protein. |
| LIN28A |
CSD |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Might also bind RNA |
| LIN28B |
CSD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Structure (PDB: 4A75) is with single stranded DNA. |
| YBX1 |
CSD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Might also bind RNA |
| YBX2 |
CSD |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Might also bind RNA |
| YBX3 |
CSD |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Identical DBD to YBX1. Might also bind RNA. |
| RBPJ |
CSL |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RBPJL |
CSL |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| CUX1 |
CUT; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CUX2 |
CUT; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ONECUT1 |
CUT; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ONECUT2 |
CUT; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ONECUT3 |
CUT; Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SATB1 |
CUT; Homeodomain |
Yes |
Known motif |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
SATBs were analyzed by Gwenael Badis and Mike Berger a decade ago; by PBMs. It did not yield a motif; instead; the signal was very closely proportional to nucleotide content, as the name suggests (Special AT Binding). |
| SATB2 |
CUT; Homeodomain |
Yes |
Inferred motif |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
|
SATBs were analyzed by Gwenael Badis and Mike Berger a decade ago; by PBMs. It did not yield a motif; instead; the signal was very closely proportional to nucleotide content, as the name suggests (Special AT Binding). |
| CXXC1 |
CxxC |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
X-ray structure (PDB:3QMI) indicates sequence specific binding through base contacts (PMID: 21407193). |
| CXXC4 |
CxxC |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds unmethylated CpG-rich sequences: (PMID: 23563267). |
| CXXC5 |
CxxC |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DNMT1 |
CxxC |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FBXL19 |
CxxC |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| KDM2A |
CxxC |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a CXXC zinc finger that recognizes CGs (PMID: 22083960) |
| KDM2B |
CxxC |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TET1 |
CxxC |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TET3 |
CxxC |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| KMT2A |
CxxC; AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Contains 3 AT-hook domain, a CXXC domain, and a possible C2H2 domain. |
| KMT2B |
CxxC; AT hook |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Structural evidence shows direct DNA-binding (PDB:4PZI) and KMT2B appears to make specific contacts with methylated DNA. |
| DMRT1 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMRT2 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMRT3 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMRTA1 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMRTA2 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMRTB1 |
DM |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
|
| DMRTC2 |
DM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| E2F1 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| E2F2 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Can also bind as a heterodimer with DP1 (PMID: 16360038) |
| E2F3 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Binds preferentially with DP proteins in vivo |
| E2F4 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| E2F5 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Also heterodimerzes with DP2 (PMID: 7760804) |
| E2F6 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| E2F7 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| E2F8 |
E2F |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFDP1 |
E2F |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| TFDP2 |
E2F |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
|
| TFDP3 |
E2F |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Interacts with E2F1; E2F2; E2F3; E2F4 and E2F5 (PMID: 17062573). |
| EBF1 |
EBF1 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EBF2 |
EBF1 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
EBF1 has a nice HT-SELEX model and based on this paper (PMID:23499423). EBF2 binds similar motif to control brown/beige fat cell identity. |
| EBF3 |
EBF1 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| EBF4 |
EBF1 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| EHF |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELF1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELF2 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELF4 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELF5 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELK1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELK3 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELK4 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ERF |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ERG |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETS1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETS2 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV2 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV3 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV3L |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ETV4 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV5 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV6 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ETV7 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Experimental low-throughput evidence of DNA-binding and changes in reporter expression (PMID: 11108721) |
| FEV |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FLI1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GABPA |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SPDEF |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SPI1 |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SPIB |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SPIC |
Ets |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ELF3 |
Ets; AT hook |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FLYWCH1 |
FLYWCH |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Several C. elegans FLYWCH domain proteins bind specific DNA sequences in Y1H and EMSA (PMID: 18794349 and PMID: 15165844). |
| FOXA1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXA2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXA3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXB1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXB2 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXC1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXC2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXD1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| FOXD2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXD3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXD4 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXD4L1 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXD4L2 |
Forkhead |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
This ENSEMBL ID has been retired. |
| FOXD4L3 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXD4L4 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| FOXD4L5 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXD4L6 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXE1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXE3 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXF1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| FOXF2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| FOXG1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXH1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Full length protein did not yield an HT-SELEX motif |
| FOXI1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXI2 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXI3 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXJ1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| FOXJ2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXJ3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXK1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXK2 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXL1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXL2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXM1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| FOXN1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| FOXN2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXN3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXN4 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| FOXO1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXO3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXO4 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXO6 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXP1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| FOXP2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXP3 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXP4 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXQ1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXR1 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXR2 |
Forkhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| FOXS1 |
Forkhead |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFYVE26 |
FYVE-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
FYVE zinc fingers are unlikely to bind DNA |
| GATA1 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATA2 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATA3 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATA4 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATA5 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATA6 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GATAD1 |
GATA |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The GATA domain is truncated (see alignment) |
| GATAD2A |
GATA |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has the full GATA domain, and JPRED4 thinks the secondary structure is preserved. The GATA domain is not sufficiently well studied to declare that specific amino acids are absolutely required in order to bind DNA. Many unusual GATA domain proteins across eukaryotes bind DNA, making it reasonable to project that this one does, too. |
| GATAD2B |
GATA |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has the full GATA domain, and JPRED4 thinks the secondary structure is preserved. The GATA domain is not sufficiently well studied to declare that specific amino acids are absolutely required in order to bind DNA. Many unusual GATA domain proteins across eukaryotes bind DNA, making it reasonable to project that this one does, too. |
| TRPS1 |
GATA |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| ZGLP1 |
GATA |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| GCM1 |
GCM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GCM2 |
GCM |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GRHL1 |
Grainyhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GRHL2 |
Grainyhead |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| GRHL3 |
Grainyhead |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds the same AACCGGTT consensus as the paralog GRHL1 based on SELEX (PMID: 21081122). |
| TFCP2 |
Grainyhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TFCP2L1 |
Grainyhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| UBP1 |
Grainyhead |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GTF2I |
GTF2I-like |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
(PMID: 18326499) shows through SELEX and EMSA that this family binds DNA specifically. Transfac motifs are dubious. |
| GTF2IRD1 |
GTF2I-like |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
(PMID: 18326499) shows through SELEX and EMSA that this family binds DNA specifically. Transfac motifs are dubious. V$BEN_02 motif has partial similarity to a shift-experiment sequence (PMID:14645227), which shows DNA-binding and evidence of transcriptional regulation by knockdown experiments |
| GTF2IRD2 |
GTF2I-like |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 18326499) shows through SELEX and EMSA that this family binds DNA specifically. |
| GTF2IRD2B |
GTF2I-like |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 18326499) shows through SELEX and EMSA that this family binds DNA specifically. |
| AC105001.2 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be sequence specific TF - it has a deletion inside the SOX-domain removing several residues that contact DNA based on the structure of paralog SOX17. |
| BBX |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CCDC124 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Based on the alignment, it lacks a proper HMG domain. Evidence it binds RNA (PMID: 22658674). |
| CHD3 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
No evidence for sequence-specific DNA-binding in the literature; and contains only a partial match to an HMG box with no similarity to DBDs of other CHD family proteins |
| CHD4 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
CHD4 is likely not a sequence-specific DNA-binding protein despite having a partial match to an HMG box. This protein binds to the DNA backbone, but binds poly(ADP-ribose) with higher affinity (PMID: 26565020). |
| CIC |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HBP1 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HMG20A |
HMG/Sox |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Similar to HMG20B, which has an inferred motif from mouse. |
| HMG20B |
HMG/Sox |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HMGB1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. Evidence exists showing HMGB1/2 are non-sequence-specific binding proteins (PMID: 11497996). |
| HMGB2 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. Evidence exists showing HMGB1/2 are non-sequence-specific binding proteins (PMID: 11497996). HMGB2 is well-known to facilitate DNA-bending and interact with sequence-specific TFs and transcriptional co-factors. |
| HMGB3 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Similar to HMGB1/2, which bind DNA with low specificity |
| HMGB4 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Similar to HMGB1/2, which bind DNA with low specificity. Yet, it can also bind with 4.35nM affinity to DNA containing an intra-strand crosslink made by cis-platin (PMID: 22901013). |
| HMGN1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. |
| HMGN3 |
HMG/Sox |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| HMGXB3 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. |
| HMGXB4 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. |
| KMT2C |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
Based on the alignment, it is quite different from all other HMG proteins. It is borderline to say that it is a HMG at all. |
| KMT2D |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Based on alignment it is quite different from all other HMG proteins, borderline to say if it is a HMG at all. Crystal structure has an aminoacid sequence that doesnt match to the protein it claims to be |
| LEF1 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MAEL |
HMG/Sox |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Orthologous protein from mouse binds RNA (PMID: 25807393) |
| NSD2 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Likely affects transcription by histone modification (not specific DNA-binding). |
| PBRM1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
(PMID: 23867514) shows it may bind nucleosomal DNA. |
| PMS1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. |
| SMARCE1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
In the alignment, it clusters with other HMG proteins that have not yielded motifs. Contributes to SWI/SNF DNA-binding (PMID: 9435219). |
| SOX1 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| SOX10 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX11 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| SOX12 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX13 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| SOX14 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX15 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX17 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX18 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX2 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX21 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX3 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX30 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX4 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also binds ssDNA loops. |
| SOX5 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX6 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX7 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX8 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SOX9 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also binds ssDNA loops. |
| SRY |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SSRP1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
HMG domain is highly divergent based on AA-sequence |
| TCF7 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF7L1 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TCF7L2 |
HMG/Sox |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| TFAM |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
HMG domain is highly divergent based on AA-sequence |
| TOX |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Predicted to be a non- or low specificity TF (PMID: 12697058). However, there is a DAM-id based motif with SSSSGNNGCG-consensus (PMID: 25527292), but this does not look like HMG-site |
| TOX2 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
TOX proteins are clearly their own distinct subfamily of HMG proteins. No strong evidence for them binding DNA specifically. |
| TOX3 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
TOX proteins are clearly their own distinct subfamily of HMG proteins. No strong evidence for them binding DNA specifically. |
| TOX4 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
TOX proteins are clearly their own distinct subfamily of HMG proteins. No strong evidence for them binding DNA specifically. |
| UBTF |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
No evidence for or against specific DNA-binding by this class of HMG box containing proteins |
| UBTFL1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
No evidence for or against specific DNA-binding by this class of HMG box containing proteins |
| WDHD1 |
HMG/Sox |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Divergent HMG motif, doesnt cluster either with specific or nonspecific HMG proteins |
| BHMG1 |
HMG/Sox; bHLH |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Based on the alignment, it lacks a proper HMG domain. bHLH domain is also highly unlike any other human bHLH TF (<40% DBD ID) |
| ADNP |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ADNP2 |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ALX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ALX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ALX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ANHX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARGFX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ARX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BARHL1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BARHL2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BARX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| BARX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| BSX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CDX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CDX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CDX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| CERS2 |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be a TF - homeodomain is heavily truncated at the N-terminus; and LASS2/CERS2 has previously been shown to be involved in ceramide synthesis (PMID:20937905). |
| CERS3 |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be a TF - homeodomain is heavily truncated at the N-terminus; and LASS2/CERS2 has previously been shown to be involved in ceramide synthesis (PMID:20937905). |
| CERS4 |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be a TF - homeodomain is heavily truncated at the N-terminus; and LASS2/CERS2 has previously been shown to be involved in ceramide synthesis (PMID:20937905). |
| CERS5 |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be a TF - homeodomain is heavily truncated at the N-terminus; and LASS2/CERS2 has previously been shown to be involved in ceramide synthesis (PMID:20937905). |
| CERS6 |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Unlikely to be a TF - homeodomain is heavily truncated at the N-terminus; and LASS2/CERS2 has previously been shown to be involved in ceramide synthesis (PMID:20937905). |
| CRX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DBX1 |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DBX2 |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DLX6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DMBX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DPRX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DRGX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| DUX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Not included in Ensembl. Binds GATCTGAGTCTAATTGAGAATTACTGTAC in EMSA (PMID: 9736770) |
| DUX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Not included in Ensembl. |
| DUX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| DUXA |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EMX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EMX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EN1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EN2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ESX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EVX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| EVX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GBX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GBX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GSC |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GSC2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GSX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GSX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HDX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HESX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HHEX |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HLX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HMBOX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HMX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HMX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HMX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HNF1A |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HNF1B |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOMEZ |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOPX |
Homeodomain |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lacks conserved residues required for DNA binding (PMID: 24287901) |
| HOXA1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA10 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA11 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also forms heterodimers with MEIS and PBX. |
| HOXA13 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HOXA4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| HOXA5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA7 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXA9 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB13 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also forms heterodimers. |
| HOXB2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB7 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXB9 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC10 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC11 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC12 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC13 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HOXC6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| HOXC8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXC9 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD10 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD11 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD12 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD13 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HOXD9 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| IRX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| IRX5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRX6 |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ISL1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ISL2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ISX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LBX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LBX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LEUTX |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| LHX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LHX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| LHX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| LHX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LHX5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LHX6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LHX8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LHX9 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| LMX1A |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LMX1B |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEIS1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEIS2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEIS3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEOX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEOX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MIXL1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MKX |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Orthologous protein from fly is a TF that binds NWACA (PMID: 22923612). |
| MNX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MSX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MSX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NANOG |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NANOGNB |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| NANOGP8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Listed as a pseudogene, but it encodes two protein products |
| NKX1-1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX1-2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX2-1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX2-2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX2-3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX2-4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX2-5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX2-6 |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX2-8 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX3-1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX3-2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NKX6-1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NKX6-2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| NKX6-3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NOBOX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NOTO |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OTP |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| OTX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| OTX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PBX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PBX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
High sequence similarity to PBX1, PBX4, and drosophila exd, which have in vitro-derived motifs |
| PBX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
High sequence similarity to PBX1, PBX4, and drosophila exd, which have in vitro-derived motifs |
| PBX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PDX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PHOX2A |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PHOX2B |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PITX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PITX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PITX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PKNOX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PKNOX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PROP1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PRRX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PRRX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RAX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RAX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RHOXF1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RHOXF2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RHOXF2B |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SEBOX |
Homeodomain |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Role in early development (PMID: 24018616). |
| SHOX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SHOX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SIX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SIX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SIX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SIX4 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SIX5 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| SIX6 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TGIF1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TGIF2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TGIF2LX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TGIF2LY |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TLX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| TLX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TLX3 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TPRX1 |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Expressed in early embryo as transcripts that contain a full homeodomain (PMID: 27412763). |
| UNCX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VAX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VAX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VENTX |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VSX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VSX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZFHX2 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ZHX1 |
Homeodomain |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| ZHX2 |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| ZHX3 |
Homeodomain |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| PAX2 |
Homeodomain; Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX3 |
Homeodomain; Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX4 |
Homeodomain; Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX6 |
Homeodomain; Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX7 |
Homeodomain; Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU1F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU2F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU2F2 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU2F3 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU3F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU3F2 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU3F3 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU3F4 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU4F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU4F2 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU4F3 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU5F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU5F1B |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU5F2 |
Homeodomain; POU |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| POU6F1 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| POU6F2 |
Homeodomain; POU |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSF1 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSF2 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSF4 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSF5 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSFX1 |
HSF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| HSFX2 |
HSF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| HSFY1 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HSFY2 |
HSF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF1 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| IRF2 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF3 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF4 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF5 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| IRF6 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF7 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF8 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| IRF9 |
IRF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LYAR |
LYAR-type C2H2 ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
LYAR-type C2H2 ZF domains have not been shown to bind DNA. LYAR binds to the 60S subunit of the ribosome. It regulates translation rather than transcription (PMID: 24990247). |
| MSANTD1 |
MADF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| MSANTD3 |
MADF |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NAIF1 |
MADF |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BORCS8-MEF2B |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| MEF2A |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEF2B |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEF2C |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MEF2D |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SRF |
MADS box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| BAZ2B |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
|
| MBD2 |
MBD |
Yes |
Known motif |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain; Has a putative AT-hook |
|
| MBD3 |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
The MBD domain of MBD3 is thought to be primarily responsible for interaction with HDAC1 and MTA2, members of the NuRD complex (PMID: 12124384). More recently, studies have shown that it retains the ability to bind methylated CpG sites in vitro (PMID: 24307175) with lower affinity than other MBD proteins (e.g., MBD2), but does not distinguish between hydroxymethylated and unmethylated sites. Coupled with in vivo ChIP experiments, it appears that MBD3 binds unmethylated CpG sites in vivo after be |
| MBD4 |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| MBD6 |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Has not been tested on PBM or HT-SELEX. Some evidence exists showing that it does not bind methylated DNA (PMID: 20700456), and the MBD domain instead facilitates protein interactions (PMID: 24634419). |
| PIN1 |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| SETDB1 |
MBD |
Yes |
Known motif |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Transfac motif is dubious. |
| SETDB2 |
MBD |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| BAZ2A |
MBD; AT hook |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Component of the silencing nucleolar remodelling complex (NoRC) (PMID: 22368283) |
| MECP2 |
MBD; AT hook |
Yes |
Known motif |
3 Low specificity DNA-binding protein |
100 perc ID - in vitro |
|
Binds methylated CpG dinucleotides (PDB: 3C2I) |
| MBD1 |
MBD; CxxC ZF |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds CpG methylated DNA (PDB: 1IG4). It is unclear how much other specificity has been defined. |
| MTERF1 |
mTERF |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
The structure (PDB: 3MVA) shows a large protein DNA-interaction interface. |
| MTERF2 |
mTERF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| MTERF3 |
mTERF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Crystral structure available (PMID: 20430012) |
| MTERF4 |
mTERF |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
MTERF4 can bind RNA (PMID: 22949673), but likely to also bind DNA like other mTERF family members. |
| NEB |
mTERF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Gene Cards/GO indicates that NEB is not present in the nucleus; and it appears to be an actin binding protein highly expressed in muscle. |
| C17orf49 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 1 SANT domain, suggesting it cannot bind DNA specifically |
| CDC5L |
Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Compelling evidence for DNA binding (PMID: 11082045). |
| CHD2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain; Has a putative AT-hook |
Although CHD2 has weak similarity to a Myb domain (PMID: 9326634), its more closely related to the non-DNA-binding SANT domain based on the alignment analysis. The data showing that show that CHD2 binding histone H3.3 (PMID:22569126) further support the conclusion that the Myb domain is probably a SANT domain facilitating the histone interaction |
| CRAMP1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a single SANT domain, no evidence for sequence-specific DNA binding |
| DMTF1 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains 2 Myb DBDs. Binds to CCCG(G/T)ATGT (PMID: 8887674) |
| DNAJC1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains |
| DNAJC2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains |
| ELMSAN1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a single SANT domain, no evidence for sequence-specific DNA binding |
| KIAA1841 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Domain is truncated, and there is nothing known about this gene |
| MIER1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a single SANT domain, no evidence for sequence-specific DNA binding |
| MIER2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
MIER2s Myb domain is more similar to the non-DNA-binding SANT domain |
| MIER3 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
MIER3s Myb domain is more similar to the non-DNA-binding SANT domain. Tested on both PBM and HT-SELEX, with no motif. |
| MIS18BP1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 1 SANT domain, and a SANTA domain |
| MSANTD4 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains a single Myb-like domain with an insertion in the middle. It is ambiguous whether Myb-like domains are DNA or protein binding. Since it has a single domain its likely non-specific. |
| MYB |
Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Contains 3 Myb DBDs |
| MYBL1 |
Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Contains 3 Myb DBDs |
| MYBL2 |
Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Contains 3 Myb DBDs |
| MYPOP |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains a single Myb-like domain. Mouse ortholog has motif |
| MYSM1 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
MYSM1 has been shown to bind DNA. This interaction requires the MYSM1 Myb but not the SWIRM domain (PMID: 17428495). Domain sequence alignment places it near DNA-binding Myb domains but scores slightly higher as a SANT rather than Myb domain based on Prosite patterns. Given that most Myb proteins that bind DNA sequence specifically have multiple Myb domains in an array, this protein could bind DNA sequence non-specifically with its single Myb domain. |
| NCOR1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains. Member of N-CoR deacetylase complex (PMID: 14527417). |
| NCOR2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains |
| PRDM11 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
SANT domain containing protein. Mouse Prdm11 contains Myb-like domain and binds DNA in PBM experiments but has low sequence identity (21%) |
| RCOR1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains. Plays a well-established co-repressor role in the histone LSD1/RCOR1 de-methylase complex. There is some evidence that the protein contacts extranucleosomal DNA (PMID: 25916846). |
| RCOR2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains |
| RCOR3 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 2 SANT domains, and no other putative DNA-binding domains. RCOR3 SANT domains are known to facilitate PPIs. Known co-repressor - likely recruited by multiple TFs, as reviewed in (PMID: 24820421). |
| SMARCA1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
SMARCA1 contains a truncated Myb-like and SANT domain. Given the presence of the Myb-like domain, and other domains known to associated with DNA (DEAD box helicase) it likely associates with DNA non-sequence-specifically |
| SMARCA5 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
Contains a SANT, and Myb-like domain. Chromatin remodeling complex component that operates in DNA repair (PMID: 24990377); interacts with DNA, but presumably in non-sequence specific manner. |
| SMARCC1 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 1 SANT domain, and no other putative DNA-binding domains. Given that SMARCC1 is part of the Swi/Snf chromatin remodelling complex, its Myb/Sant domain is likely involved in binding histone tails. Available motif logos ares likely specificifities of SMARCC1 interactors. |
| SMARCC2 |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains 1 SANT domain, and no other putative DNA-binding domains. Available motif logos ares likely specificifities of SMARCC2 interactors. |
| SNAPC4 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
EMSA data available showing it can specifically bind DNA (PMID: 9418884) |
| TADA2A |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
TADA2A contains a single SANT domain and is thus unlikely to bind DNA |
| TADA2B |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
TADA2B contains a single SANT domain and is thus unlikely to bind DNA |
| TERB1 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains a single Myb domain (with slightly less similarity to a SANT domain). This domain has been shown to be involved in PPIs (PMID: 24413433), but this may not be mutually exclusive with DNA-binding. |
| TERF1 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains 1 Myb domain, and has structural evidence of DNA-binding (PDB: 1IV6). Subunit of Shelterin, a complex that specifically binds telomeres (PMID: 16166375). |
| TERF2 |
Myb/SANT |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
The sequence in the crystal structure (PDB:1VFC), GTTAGGGTTAGGG, matches the inferred mouse motif. |
| TERF2IP |
Myb/SANT |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a single Myb-like domain. Forms a complex with TERF2, where it modulates the binding of TERF2 to telomeres (PMID: 25675958). Unclear if TERF2IP contacts DNA directly. |
| TTF1 |
Myb/SANT |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Contains Myb and Myb-like domains, and is annotated as a Pol1 terminator. DNA-binding has been demonstrated in vitro via EMSA (PMID: 7597036). |
| ZZZ3 |
Myb/SANT |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Contains 1 Myb DBD |
| MTA1 |
Myb/SANT; GATA |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains a GATA and SANT domain. Unclear whether the GATA domain is a bona fide DBD as the MTA/RERE family domains are atypical to human GATA domains (see alignment). In CIS-BP there is one protein from C.elegans that shares domain homology and binds a GATA motif (elg-27, ChIP-seq). The GATA ZnF domain of MTA1 is required for its interaction with RBBP4 and RBBP7 (PMID:18067919). Full-length protein has been tried in HT-SELEX and did not yield a motif |
| MTA2 |
Myb/SANT; GATA |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains a GATA and SANT domain. Unclear whether the GATA domain is a bona fide DBD as the MTA/RERE family domains are atypical to human GATA domains (see alignment). In CIS-BP there is one protein from C.elegans that shares domain homology and binds a GATA motif (elg-27, ChIP-seq). Full-length protein has been tried in HT-SELEX, and DBD has been tried on PBM - neither yielded motifs |
| MTA3 |
Myb/SANT; GATA |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains a GATA and SANT domain. Unclear whether the GATA domain is a bona fide DBD as the MTA/RERE family domains are atypical to human GATA domains (see alignment). In CIS-BP there is one protein from C.elegans that shares domain homology and binds a GATA motif (elg-27, ChIP-seq). Hasnt been tried in any in vitro assays |
| RERE |
Myb/SANT; GATA |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains a GATA and SANT domain. Unclear whether the GATA domain is a bona fide DBD as the MTA/RERE family domains are atypical to human GATA domains (see alignment). In CIS-BP there is one protein from C.elegans that shares domain homology and binds a GATA motif (elg-27, ChIP-seq). Has been tried as a DBD in HT-SELEX but did not yield a motif |
| ZMYM1 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ZMYM2 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ZMYM3 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The cassette of seven znf-MYM domains are used to bind SUMO (PMID: 25133527). Overall, very little is known about this domain or protein. |
| ZMYM4 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lacks a canonical DBD |
| ZMYM5 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Binds to and represses activity of ETV5 based on (PMID: 17126306), but there is no evidence for it binding the DNA itself, so it seems like an co-repressor |
| ZMYM6 |
MYM-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Truncated BED ZF |
| ZMYND10 |
MYND-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MYRF |
Ndt80/PhoG |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Mouse ortholog binds a highly similar motif. |
| MYRFL |
Ndt80/PhoG |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Related to other MYRF TFs, which have related PBM motifs |
| NFX1 |
NFX |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| NFXL1 |
NFX |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Likely a TF based on presence of NFX ZF. |
| ZNF330 |
NOA36-type ZF |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein has IPR010531 domain, Zinc finger protein NOA36, which has not been shown to bind DNA |
| AR |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ESR1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ESR2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| ESRRA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ESRRB |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| ESRRG |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HNF4A |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| HNF4G |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| NR0B1 |
Unknown |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| NR1D1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR1D2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR1H2 |
Nuclear receptor |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Likely an obligate heteromer (PMID: 7935418; PMID: 7892230; PMID: 7744246) |
| NR1H3 |
Nuclear receptor |
Yes |
Inferred motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Binds as an obligate heterodimer with RXR-proteins. (PDB: 2ACL) is a crystal structure of the two proteins without DNA |
| NR1H4 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Also binds DNA as heterodimer with RXRA (PMID: 11870371) |
| NR1I2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR1I3 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2C1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2C2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2E1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2E3 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2F1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR2F2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| NR2F6 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR3C1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR3C2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR4A1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR4A2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR4A3 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| NR5A1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR5A2 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NR6A1 |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PGR |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PPARA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| PPARD |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PPARG |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Also heterodimerizes. |
| RARA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RARB |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RARG |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RORA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RORB |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RORC |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RXRA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RXRB |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Has been shown to bind both as a homodimer and with several nuclear receptor homodimerization partners |
| RXRG |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Usually binds in vivo as a heterodimer, but can bind as a homodimer in vitro |
| THRA |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Likely binds as a heterodimer too |
| THRB |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| VDR |
Nuclear receptor |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| AATF |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely does not bind to bind to DNA (PMID: 17634135). |
| ABL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ABRA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The Costars domain in this protein is an atypical winged helix protein that does not bind DNA but to other proteins (PMID: 21082705) |
| AC020915.1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ACOD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ACTR3B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ACTR3C |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Pfam match to an APSES domain - this is likely a false positive, as these domains are mostly present in bacteria and fungi |
| ADAM8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ADAMTS17 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ADAMTS19 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| ADAR |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
PMID: 21728134 shows the ADAR protein bind to ds RNA and Z DNA. At best it would be a non-sequence specific DNA binding protein. But, it has a well established role as a dsRNA binding protein, so it is unlikely to be a TF. |
| ADGRA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ADGRG3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| AEBP1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
This is a protease, but its ability to bind DNA is supported by both gel-shift (PMID: 15654748) and ChIP (PMID: 22723309). |
| AES |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely a transcriptional co-factor |
| AFAP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
There is no evidence suggesting DNA-binding activity |
| AFF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
MLL fusion partner |
| AFF3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 8555498) only says that In vitro-translated LAF-4 was able to bind strongly to double-stranded DNA cellulose - thats more consistent with nonspecific DNA binding. The key issue is whether the Transcription factor AF4/FMR2 (IPR007797) domain really is sequence specific. Most of the work has been done on the one Drosophila ortholog, lilliuputian. I see no evidence of DNA binding. Recent work on this family in human indicate that it functions in coactivation (PMID: 27899651; PMID: 261712 |
| AFF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 8555498) only says that In vitro-translated LAF-4 was able to bind strongly to double-stranded DNA cellulose - thats more consistent with nonspecific DNA binding. The key issue is whether the Transcription factor AF4/FMR2 (IPR007797) domain really is sequence specific. Most of the work has been done on the one Drosophila ortholog, lilliuputian. I see no evidence of DNA binding. Recent work on this family in human indicate that it functions in coactivation (PMID: 27899651; PMID: 261712 |
| AGER |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contacts DNA in the structure (PDB: 4OI7) |
| AGT |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| AIM2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Based on (PDB: 3RN2), the protein binds DNA but contacts only the backbone; AIM2 binds cytrosolic dsDNA in the innate immune response |
| AKT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ALK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates far upstream in the signaling cascade |
| ALKBH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Dioxygenase that repairs alkylated DNA and RNA containing 1-methyladenine and 3-methylcytosine by oxidative demethylation. Binds DNA in the crystal structure (PDB: 3BTX) |
| AMH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ANAPC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Scaffolding protein that associates with ubiquitin ligase complexes |
| ANKRD30A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
GO citation (PMID: 11280766) has no evidence of DNA-binding activity and was based on homology |
| ANXA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein operates far upstream on the signaling cascade. |
| ANXA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| AP5Z1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
May have helicase activity and play a role in DNA repair (PMID: 20613862) |
| APBB3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| APEX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
The structure (PDB:1DEW) is with abasic DNA - the protein is a base excision repair enzyme that cleaves off abasic bases |
| APOBEC3A |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds ssDNA (PDB: 5KEG) |
| APOBEC3B |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds ssDNA (PDB: 5TD5) |
| APOBEC3G |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Restriction factor of HIV-1 that binds ssDNA (PDB: 5K83) |
| APTX |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds and fixes DNA-RNA hybrids/ APTX efficiently repairs adenylated RNA-DNA and acts in the RNA-DNA damage response (PMID: 24362567) |
| ARHGAP35 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds DNA specifically based on EMSA and nuclease protection assay data (PMID: 1894621), despite lacking any clear DBDs. |
| ARHGEF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ARHGEF5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO annotation provides no evidence of DNA-binding activity (PMID: 15601624) |
| ARRB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ChIP data available, but unclear if it can bind to DNA directly (PMID: 16325578) |
| ARRB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ASCC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a coactivator that is reported to bind to SRF, NFKB1, and JUN (PMID: 12077347) |
| ATF7IP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Murine homolog involved in H4K9 trimethylation by SETDB1 (PMID: 14536086) |
| ATM |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase protein that binds to and activates certain TFs |
| ATR |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| ATRX |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
ATRX does not contain any canonical sequence-specific DBDs but it does contain a non-specific DNA binding helicase that allows it to bind repeat sequences (PMID:21029860) and telomeres (PMID:20651253). ATRX is involved in multiple processes (transcription, replication), and is associated with multiple complexes (Swi/Snf, histone chaperones, and repressive complexes including TRIM 28 (PMID:27029610)), and as such does affect transcription. Given the lack of sequence-specific binding it is unlikel |
| ATXN7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ATXN7 SCA7 domain facilitates interactions with histone dimers (PMID: 20634802) |
| BAG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Antiapoptotic BCL-protein |
| BANF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure, contacting only the backbone from the side of the minor groove (PDB: 2BZF) |
| BANP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
BANP has no DBD and is known to bind other TFs; likely that the Transfac motif is from one of its binding partners |
| BCL10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Apoptosis associated protein that operates upstream on a cascade that includes NFKB |
| BCL3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
No DBD - instead, this is a known cofactor of NF-kappaB. The Transfac motif is the NFKB1 motif. GO cites only electronic annotation and needs to be fixed. |
| BCLAF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
No DBD. Only weak evidence is available for indirect binding (PMID: 10330179). Suspect motif - it is a clear ETS-site. (PMID: 10330179) shows that the protein binds DNA in filter binding assay, but not that it is sequence specific. |
| BCOR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-repressor that associates with BCL6 (PMID: 10898795) |
| BDP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BEX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely a cofactor- (PMID: 16314316) shows results for related BEX2 |
| BIN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BLM |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Helicase involved in DNA replication and repair (PDB: 4CGZ) |
| BLZF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is a golgi protein with no evidence for DNA binding. |
| BMI1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
BMI1 binds to nucleosomes as part of the PRC1 complex but does not contact the DNA directly (PDB: 4R8P) |
| BMP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BMP4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely a cofactor. |
| BMP7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BMPR1A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BOD1L1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| BOLA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BOLA2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BOLA2B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BOLA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
E. Coli homologue of the BOLA binds DNA; however there is no evidence in the mammalian proteins |
| BPNT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BPTF |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain; Has a putative AT-hook |
(PMID: 10575013) obtained a motif by SELEX and showed that mutating the sequence diminished binding in vitro. Unusual for a PHD/Ring finger, but its there in the literature. |
| BRCA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
|
BRCA1 likely binds to DNA without DNA sequence specificity (PMID: 11353843) |
| BRD4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Binds acetylated histones |
| BRD7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BRD8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
TF-coactivator |
| BRD9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Evidence ony for interaction with histones (PMID: 22464331) |
| BRF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
GTF - Pol III - TRANSFAC has a motif but its likely not for this protein, but for the complex as a whole |
| BRF2 |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Makes backbone and sequence-specific interactions with DNA (PDB: 4ROC), but only involved in recognizing dinucleotides flanking the TATA box (PMID: 26638071). Redox sensing determines activation and repression of target genes |
| BRMS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
BRMS1 functions as a corepressor by promoting binding of HDAC1 to RelA/p65, where it deacetylates lysine K310 on RelA/p65, which suppresses RelA/p65 transcriptional activity (PMID: 17000776) |
| BRPF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| BTAF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein that uses ATP to dissociate TBP from the promoter |
| BTBD8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Probably annotated as TF based on presence of a BTB domain; however, these domains are not known to bind DNA |
| BTG2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-factor (PMID: 10617598) |
| BTK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Involved in the regulation of ARID3A and NFAT in B lymphocyte development; has been thoroughly investigated, but there is no evidence to demonstrate DNA binding activity (see UniProt Q06187) |
| BTRC |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| BUD31 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included because GO says its DNA binding on the basis of (PMID: 7841202), a 1995 paper that only suggests DNA binding on the basis of the protein sequence. In fact, it is composed entirely of a G10 domain. |
| C14orf39 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| C1D |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
C1D has been shown to bind RNA (PMID: 17412707) and is associated with the exosome. C1D is also associated with DNA repair and has DNA-binding activitiy (PMID: 10362552) |
| C20orf194 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| C3orf33 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Some effect on DNA-binding of AP-1 (PMID: 20680465), but does no data supporting a role for C3orf33 as a DNA-binding factor itself |
| CACTIN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein operates on a signaling cascade far upstream of NFKB (PMID: 20829348) |
| CAMK1D |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Functions in signalling cascade that leads to phosphorylation and activation of CREB (PMID: 16324104) |
| CAMK2A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CAPN15 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Basically an unknown protein - a likely protease that contains also znfRANBP-domains, so it could be a RNA-binding protein |
| CAPN3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because GO says positive regulation of NF-kappaB transcription factor activity. No indication of sequence specific DNA binding. |
| CARD11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Plasma-membrane protein possibly functioning in upstream signaling of NFKB (PMID: 12154360) |
| CARD14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CARF |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Transfac-only motif. Major evidence is found in (PMID: 11832226). Cloned by Y1H and binding demonstrated by gel-shift. Mutant probes do not compete. DNA binding ability seems solid but motif is sketchy. |
| CASP8AP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Pfam DBD match is a likely false-positive - did not produce a motif in PBM experiments |
| CAT |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that breaks down hydrogen peroxide |
| CBFA2T2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
CBFA2T2 oligomerizes to form a scaffold upon which PRDM14 and OCT4 are stabilized on chromatin (PMID: 27281218) |
| CBFA2T3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Co-repressor - does not contact DNA (PMID: 12559562; PMID: 15203199) |
| CBFB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
CBFB augments the binding of RUNX to DNA, but does not itself bind DNA. Thus; it is a cofactor. Reviewed in (PMID:11105900). Two citations used by GO (PMID:8351518; PMID:9751756) do not demonstrate DNA binding. |
| CBL |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiquitin ligase |
| CBLL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
E3-ubiquitin ligase involved in the regulation of cell adhesion (PMID: 11836526) |
| CC2D1A |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 17714190) states that human Freud-1L bound specifically to its dual repressor element in the 5-HT1A receptor gene in vitro |
| CC2D1B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 19423080) says it binds a known locus in vivo, although lack of canonical DBDs suggests indirect DNA-binding |
| CCDC71 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| CCNT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
General transcription machinery required to stimulate RNA pol II elongation (PMID: 16109377) |
| CCNT2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Has low or no sequence specificity (PMID: 27899659) |
| CD36 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CD40 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Cell surface receptor of TNF-family |
| CD40LG |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CDC6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CDK5RAP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CDK7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CDK8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Mediator component |
| CDK9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase protein. There is a structure with RNA (PDB: 5L1Z), where the CDK9 does not contact the RNA |
| CDKN1A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CDKN2A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein binds to and inactivates NFKB1 (PMID: 10353611) |
| CEBPZ |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| CELF3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Is a well established RBP |
| CENPA |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone like protein. Binds DNA in the crystal structure (PDB: 3AN2). |
| CENPS |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4NDY) in heterodimeric complex with CENPX. Protein complex has many contacts with the backbone, but only a few with the bases. |
| CENPT |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contains an archaeal histone-like fold (CBF_NFY). but at best would have low sequence specificity. Known role in centromere assembly and lack of known sequence specificity suggest that it is unlikely to be a sequence specific TF. |
| CENPX |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4NDY) in heterodimeric complex with CENPS. Protein complex has many contacts with the backbone, but only a few with the bases. |
| CFLAR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CGGBP1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds unstable triplet repeat 5-d(CGG)n-3 in the human FMR1 gene (PMID: 9201980) |
| CHCHD3 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Alias FLJ20420 can specially bind the hBAG-1 promoter region by EMSA and ChIP assays (PMID: 22567091) |
| CHD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
(PMID: 22033927) discusses and presents a crystal structure with DNA. The Chd1 chromatin remodeler possesses a C-terminal DNA-binding domain that is required for efficient nucleosome sliding and believed to be essential for sensing the length of DNA flanking the nucleosome core. Recognizes backbone only, so it has low specificity. |
| CHD6 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
ATP dependent helicase (PMID: 17027977), so it has some affinity for DNA |
| CHD7 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Helicase and chromodomain |
| CHD9 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
|
| CHP1 |
Unknown |
No |
ssDNA/RNA binding |
3 Low specificity DNA-binding protein |
No motif |
|
According to EMSA, binds RNA strongly, and dsDNA weakly (PMID: 22727667) |
| CHRAC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| CHUK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase that operates upstream in the signalling cascade that leads to NFKB |
| CHURC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Most recent work has conclusively shown it does not bind DNA (PMID: 17610897), refuting a previous study (PMID: 14651851) |
| CIB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CIITA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Chromatin modifier |
| CIR1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CITED1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known co-activator. GO says its sequence-specific DNA binding transcription factor activity NAS - PMID: 8901575 but this reference does not show this. |
| CITED2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CITED4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-factor |
| CIZ1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Presence of zf-C2H2_jaz domain suggests that its likely a dsRNA binding protein |
| CLU |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because GO says positive regulation of NF-kappaB transcription factor activity, but there is no DBD and no evidence of DNA binding. |
| CMKLR1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a G protein-coupled receptor for the chemoattractant adipokine chemerin |
| CNBP |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
CNBP has a specificity for single-stranded DNA (PMID: 2562787) |
| CNOT3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Part of complex that de-adenylates mRNA molecules (PMID: 27746116) |
| CNOT4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Regulates transcription through ubiquitination of TFIID (PMID:11823428). Only contains RRM domains, with no DBDs. |
| CNOT7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID:9820826) does not support DNA-binding |
| CNOT8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Deadenylase that probably regulates genes post-transcriptionally by controlling mRNA stability (PMID: 19605561) |
| COMMD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| COMMD6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| COMMD7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| COPS2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| COPS3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase that phosphorylates JUN and possibly other TFs |
| COPS4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CPEB1 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
HT-SELEX motif could be an artefact of ssDNA binding activity, as CPEB1 is a well-characterized RNA-binding protein. Could not find evidence of CPEB1 DNA-binding activity in the literature |
| CREBBP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
CREBBP is a likely transcriptional co-activator based on its domains and previous experimental evidence. It has previously been shown to not bind DNA sequence-specifically (PMID: 21539536) |
| CREG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Regulates transcription in tethering assays (PMID: 9710587). Unlikely to be a TF, based on the lack of a canonical DBD |
| CRTC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CRTC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
CRTC2 binds CREB and does not make contacts with the DNA (PDB: 4HTM; PMID: 23213254) |
| CRTC3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Evidence showing that CRTC2, which resembles CERTC3, lacks DNA-binding acitvity. Its reasonable to speculate CRTC3 also lacks ability to bind to DNA |
| CSRNP1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
All three paralogs (CSRNP1, CSRNP2, and CSRNP3) bind an AGAGTG consensus based on SELEX experiments (PMID: 17726538) |
| CSRNP2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
All three paralogs (CSRNP1, CSRNP2, and CSRNP3) bind an AGAGTG consensus based on SELEX experiments (PMID: 17726538) |
| CSRNP3 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
All three paralogs (CSRNP1, CSRNP2, and CSRNP3) bind an AGAGTG consensus based on SELEX experiments (PMID: 17726538) |
| CTBP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Transfac-only motif with no clear source. This is a known corepressor with a primary function in the Golgi. |
| CTBP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CTH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CTNNB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
This is beta catenin - acts as co-factor with TCF/LEF |
| CTNNBIP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CUL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Component of the E3-ubiquitin ligase complex (PMID: 11961546) |
| CUL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CUL3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CUL4A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CUL4B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Structure (PDB: 4A0L) shows that CUL4B is recruited to DNA and does not make direct contact with it |
| CUL5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CYLD |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CYP1B1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| CYTL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DAB2IP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DACH1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Binds with consensus AAWANAAAWAAWT and AATACAATTAAAT as strongest target sequences based on EMSA and SELEX (PMID: 20351289). Protein contains a winged helix structural domain (PMID: 12057194) |
| DACH2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Related to DACH1, which can bind DNA based on EMSA and SELEX (PMID: 20351289). Yet, the fly ortholog has been extensively studied and cannot bind DNA. (PMID: 8431945; PMID: 7821215) |
| DAP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein functions in apoptotic signaling |
| DAXX |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-repressor |
| DCP1A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DDB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
DDB1 does not contact the DNA in the structure (PDB: 4E5Z) - contact is mediated by DDB2 |
| DDB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DDB2 contacts the DNA in the (PDB: 4A0K) structure, albeit likely in a non sequence specific manner |
| DDN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| DDR2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DDRGK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DDX3X |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a RNA-helicase that can however bind both RNA and DNA (PMID: 21589879). The interaction is presumably nonspecific and a portion of the DNA has to be single-stranded |
| DDX5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor (PMID: 15298701) |
| DDX58 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DEK |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
This protein binds to cruciform and superhelical DNA and induces positive supercoils into closed circular DNA, and is also involved in splice site selection during mRNA processing. (Entrez gene summary). So it must have some nonspecific DNA affinity. |
| DEPDC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Interacts with transcriptional corepressor ZNF224 (PMID: 20587513) |
| DEPDC1B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein does not have known DBDs and has been shown to function as an inhibitor of a RhoA-based signaling complex (PMID: 25458010) |
| DEPDC4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DEPDC5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DEPDC7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because Vasquerizas 2009 includes it with an x. No DBD and no other data to support being a TF. |
| DEPTOR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DHX34 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DHX36 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 2N21) |
| DISP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DMAP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Component of the NuA4 histone acetyltransferase (HAT) complex, which is involved in transcriptional activation of select genes, principally by acetylation of nucleosomal histones H4 and H2A (PMID: 14966270). (PMID: 20864525) shows DNA binding is sequence independent. |
| DMC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DMRTC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This particular DM protein lacks the DM DBD (PMID: 16488114) |
| DNA2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Helicase involved in genome integrity. Binds single stranded DNA in the structure (PDB: 5EAN) |
| DNAJA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein functions in a chaperone complex |
| DNAJC21 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Contains a single Matrin-type or U1-type C2H2 domain, which typically binds dsRNA. Its a known heat shock protein that may also be involved in rRNA processing. |
| DNMT3A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNMT3A and DNMT3B are de novo methyltransferases that are activated by enzymatically inactive paralog DNMT3L. Besides the C-terminal catalytic core, the PWWP domain of 3A and 3B can also bind to DNA. Presumably there is no sequence specificity and instead the de novo methylation complexes are recruited by histone modifications on the N-terminal tail of H3. Reviewed in (PMID: 27826835). |
| DNMT3B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNMT3A and DNMT3B are de novo methyltransferases that are activated by enzymatically inactive paralog DNMT3L. Besides the C-terminal catalytic core, the PWWP domain of 3A and 3B can also bind to DNA. Presumably there is no sequence specificity and instead the de novo methylation complexes are recruited by histone modifications on the N-terminal tail of H3. Reviewed in (PMID: 27826835). |
| DNMT3L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
DNMT3A and DNMT3B are de novo methyltransferases that are activated by enzymatically inactive paralog DNMT3L. Besides the C-terminal catalytic core, the PWWP domain of 3A and 3B can also bind to DNA. Presumably there is no sequence specificity and instead the de novo methylation complexes are recruited by histone modifications on the N-terminal tail of H3. Reviewed in (PMID: 27826835). |
| DNTT |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 4I27) |
| DPF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No evidence for DNA-binding activity - possible role in transcriptional regulation complex (PMID: 16785614) |
| DR1 |
Unknown |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
Binds DNA as a heterotrimeric complex of TBP, DR1, and DRAP1 (PDB: 1JFI) |
| DRAP1 |
Unknown |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
Based on structure (PDB: 1JFI), it forms the obligate heterodimer DR1-DRAP1 that furthermore contacts TBP. Only makes contact with the minor groove in a histone-like interaction, which is probably non-specific (PMID: 11461703) |
| DSP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DTX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This protein is an E3 ligase that operates in the Notch pathway |
| DUSP12 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DVL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DVL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
DVL2 does not have any known DBDs; or experimental evidence to suggest it is a TF. |
| DVL3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| DZIP1L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a weak ProSite match for a single C2H2 ZF (Uniprot) but not a Pfam match. No experimental evidence for DNA-binding exists |
| EAF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No convincing evidence that this protein binds DNA with any sequence specificity, or that this activity is required for its function. Thus at best the current evidence is that it is a cofactor of some sort cofactor (PMID: 12446457) |
| EDA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Cell surface protein that can be cleaved into a secreted one |
| EDA2R |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because GO says positive regulation of sequence-specific DNA binding transcription factor activity. Not DNA binding. |
| EDF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known co-factor that binds DNA indirectly through interactions with TFs (PMID:12040021) |
| EDN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that is processed into a secreted signaling peptide |
| EED |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Affects transcription by histone modification (PMID: 16357870) |
| EGLN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EID1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EID2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Associates with histone deacetylases (PMID: 12586827) |
| EIF2AK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EIF2AK4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EIF3C |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EIF3CL |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EIF3K |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EME1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4P0P) in a heterodimeric complex with MUS81. |
| ENO1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Enolase - DNA binding not shown to be direct |
| EP300 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
p300 is an archetype cofactor. It has many motifs, presumably because many TFs recruit it. Does not contact DNA in the structure (PDB: 3P57) |
| EP400 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
Has a putative AT-hook |
Protein is a nucleosome remodeling complex component with a role in depositing the H3.3 variant histone into promoter and enhancer regions (PMID: 26669263). Its MYB-like and helicase domains are likely non-specific DNA binding domains |
| EPHA5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| EPM2AIP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that binds and regulates glycogen synthase allosterically (PMID: 24142699) |
| ERBIN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ERC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ERCC3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 5IY6). Protein is an ATP-dependent 3-5 DNA helicase, so likely non-specific. |
| ERCC4 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds ssDNA at splayed DNA (PDB: 2KN7) |
| EWSR1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| EXO1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Makes contact with ssDNA bases at DNA breaks (PDB: 3QE9) |
| EXOC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Plasma-membrane protein functioning in targeting of exocytic vesicles |
| EXOG |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Endo/exonuclease (5-3), endonuclease G-like. Binds DNA in the crystal structure (PDB: 5T4I), presumably non-specifically |
| EZH1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Classic polycomb protein. |
| EZH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is a classic polycomb protein with no evidence of sequence specific DNA binding after years of intense study. I dont see anything in (PMID :15520282) that supports DNA binding. |
| FAAP24 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA backbone from the side of the minor groove in the crystal structure (PDB: 4BXO) |
| FAM153C |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FAM171B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| FAM200A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein of unknown function that is conserved in animalia. Has similarities to transposases and zinc fingers, and thus could be a DNA binding protein although there is no evidence supporting this |
| FAN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
FANCD2 and FANCI associated nuclease 1. Binds DNA in the crystal structure (PDB: 4REA), presumably non-specifically |
| FANCA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Involved in DNA repair (PMID: 8896564) |
| FANCD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
DNA repair protein. Inconclusive data supporting sequence-specific binding. Binds NFKB target sites in EMSA using 293T expressing FANCD2 (PMID: 21912593). Since the protein is expressed in mammalian cells, it could still be NFKB mediated binding. |
| FANK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Binds JUN to control its activity (PMID: 20978819), but there is no evidence that it binds DNA itself |
| FARSA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FARSB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
tRNA synthetase |
| FBN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FBXO41 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FEN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in DNA replication. Binds DNA in the crystal structure (PDB: 3Q8K), presumably in a non-specific manner. |
| FER |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FGD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FHL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
LIM ZF proteins are unlikely to bind DNA. Experimental evidence does not support a role for FHL2 as a sequence-specific DNA-binding protein (PMID:10654935) |
| FLNA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Go annotation is based on (PMID: 15684392), which shows that it binds FOXC1 and PBX1 but doesnt show evidence for binding to DNA |
| FMNL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FUBP1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
ssDNA binding protein with crystal structure demonstrating binding to ssDNA (PDB: 1J4W). Its a KH domain protein - this is Levens protein, known to impact the Myc promoter. |
| FUBP3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Can bind single stranded DNA in a sequence specific manner (PMID: 8940189). Contans KH domains and has direct evidence it is an RNA-binding protein (PMID: 21252297) |
| FUS |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
FUS is a well-established RNA-binding protein |
| FZD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FZD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transmembrane receptor protein that operates far upstream in the signalling cascade |
| FZD4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| FZD6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GABPB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Evidence exists showing that GABPB1 (E4TF1-47/53) has no DNA binding activity, but can assocaite with GABPA (E4TF1-60; Ets factor) (PMID: 8441384). Crystal structure of GAPBP1 with GABPA (PDB: 1AWC) clearly shows that the protein makes an extensive protein-protein interaction with GABPA, but does not bind DNA. Transfac PWM is a clear ETS-motif, so GABP1 is unlikely to contact DNA directly |
| GABPB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Obligate heteromer with GABPB1 (the alpha subunit) (PMID: 8810337), which together interact with GABPA (PMID: 8441384), but neither contacts the DNA |
| GADD45A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Doesnt have any DBDs - likely a co-factor |
| GAS6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GAS7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 9736752) only shows that it has a proline-rich domain similar to the one in Oct2. No evidence of DNA binding. |
| GCFC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
There is some evidence that this protein is an RNA-binding protein (PMID: 24304693). |
| GEN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Resolves Holliday junctions. Binds DNA in the crystal structure (PDB: 5T9J) |
| GLMP |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds GATCCGCCCGCTTGTGGCCAACTGGCTCCAGTCAC dsDNA based on EMSA (PMID: 18021396) |
| GOLGB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Golgi resident transmembrane protein that regulates glycosylation of other proteins (PMID: 27226319) |
| GON4L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Prosite identifies a low-confidence Myb-like domain (e.g., cant decide between Myb, SANT, or no DBD), so its probably not a TF |
| GPATCH8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GPBP1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Solid data presented in (PMID: 14612417) Also known as Vasculin. (PMID: 26156556) also claims it has an extended AT hook. |
| GPBP1L1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Possible TF based on similarity to GPBP1. Despite its name, no available evidence for DNA binding. Could also be an RBP according to this screen (PMID: 22658674) |
| GPER1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GPR155 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GREM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GRM6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GTF2A1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
General transcription factor. Binds DNA in the crystal structure (PDB: 5FUR). The protein contacts the DNA backbone as a heterotrimeric complex that also includes GTF2A2 and TBP. Has an extensive protein-protein interaction interface with the GTF2A2 (that does not contact the DNA) and will probably do nothing without it |
| GTF2A1L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| GTF2A2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
GTF2A2 makes contacts with the DNA backbone (PDB:1NVP; PMID: 12972251), and thus is unlikely to be sequence-specific |
| GTF2B |
Unknown |
Yes |
Known motif |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Contacts both DNA and TBP in the structure (PDB: 1C9B) |
| GTF2E2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
GTF2E2 weakly binds dsDNA (PMID: 10716934) - unlikely to be sequence-specific |
| GTF2F1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5IY6) |
| GTF2F2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
The protein contacts DNA in the structure (PDB: 5IY6), and could thus have some specificity; DNA is contacted by domain folded from RKKKEDGKRARADKQHVLDMLFSAFEKHQYYNLKDLVDITKQPVVYLKEILKEIGVQNVKGIHKNTWELK. |
| GTF2H1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
General transcription factor |
| GTF2H2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GTF2H2 (p44) is part of the TFIIH complex, but does not contact the DNA based on structural evidence (PDB: 5IVW) |
| GTF2H2C |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a transcriptional co-regulator (PMID: 9880511) |
| GTF2H3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Pre-initiation complex component that does not contact DNA in the structure (PDB: 5IVW) |
| GTF2H4 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
General transcription factor |
| GTF3C1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Component of RNA polymerase III. Binds weakly to the A-box (PMID: 8164661) |
| GTF3C2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
GTF3C2 is a general transcription factor of RNA polymerase III and there is no evidence that it binds DNA in the preinitiation complex. Transfac motifs are suspect |
| H1F0 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone. Likely a false-positive Pfam match based on the similarity of Forkhead domains to H1 domains |
| H1FOO |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Variant linker histone protein that is expressed in oocytes |
| H1FX |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone component |
| HAVCR2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HCFC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is recruited to promoters by THAP11 and ZNF143 and probably does not bind DNA by itself (PMID: 26416877) |
| HCK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Inhibits TP73-mediated transcription activation (PMID: 17535448) |
| HDAC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Histone deacetylase; likely to be a transcriptional cofactor. Transfac motif is dubious, and the GO annotation (PMID: 8646880) seems to be based on remote homology to a yeast TF |
| HDAC10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HDAC8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HDAC9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely to be a transcriptional cofactor |
| HELZ2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HIPK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor that can act as a coactivator or corepressor. Phosphorylates many transcription factors. (UniProt Q9H2X6) |
| HIRA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Histone chaperone - TUP1 homolog. |
| HIST1H1A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone component |
| HIST1H1B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Linker histone. To my knowledge there has been no demonstration of sequence specificity of linker histones, so I think this one should be called unlikely. |
| HIST1H1C |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| HIST1H1D |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Linker histone that binds DNA as heteromeric complex with the other histone proteins |
| HIST1H1E |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA as heteromultimeric complex |
| HIST1H1T |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| HLA-DQB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HLA-DQB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HLA-DRB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HLA-DRB3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HLA-DRB5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HLTF |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
DNA repair protein. Even though it has 3 motifs, there is no compelling evidence that it really binds dsDNA - only single stranded DNA |
| HMOX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Well characterized enzyme with no additional domains. Included only because GO lists it as a regulator of TFs. No support for DNA binding activity. |
| HNRNPA1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 1PGZ) |
| HNRNPA3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a well established RBP |
| HNRNPAB |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
HNRNPAB proteins are involved in pre-mRNA splicing. However; RRM domains can also constitute ssDNA binding domains |
| HNRNPCL2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a well established RBP |
| HNRNPD |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 1WTB) |
| HNRNPDL |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a well established RBP |
| HNRNPK |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a well established RBP |
| HNRNPL |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
HNRNPL is a well-established RNA-binding protein; and the DNA-binding evidence was neither shown to be specific or direct (PMID: 11809897) |
| HNRNPU |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds pre-mRNA in vivo and binds both RNA and ssDNA in vitro (PMID: 1628625) |
| HP1BP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone H1-like protein. Binds in ChIP experiments (PMID: 27425409) and binds DNA (likely non-specifically) with HP1. |
| HR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
JmjC domain is not a DBD, and GO annotation is based on homology to a zinc finger motif and not experimental DNA-binding evidence (PMID: 9445480) |
| HSBP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that has been shown to bind to HSF1 leading to inhibition of its trimerization and DNA-binding( PMID: 9649501). |
| HSPA1A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| HSPA1B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ICAM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IFI16 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Recognizes DNA without sequence specificity (PMID: 22618232; PMID: 18472023) |
| IFNB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IGHM |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IKBKB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IKBKG |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein binds to NFKB1 to regulate its activity |
| IL10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IL1B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IL1RAP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IL4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Extracellular signaling molecule. Included as a candidate only because it regulates STAT. |
| IL5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IL6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| INF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| ING4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Interacts physically with p53 (PMID: 12750254). Transfac motif is derived from ChIP-Chip data, so unclear if it can directly bind DNA |
| INS |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IRAK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IRAK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IRAK3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IRF2BP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ITCH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ITGB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ITGB3BP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| IZUMO2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
IZUMO is not considered to be a DNA-binding domain |
| JADE1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
FYVE and PHD zinc fingers are unlikely to specifically-bind DNA |
| JAK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is JAK from the classic JAK-STAT pathway. It is included only because GO lists it under positive regulation of sequence-specific DNA binding transcription factor activity. No evidence of sequence specificity - the STATs handle that. |
| JMY |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Coactivator protein that associates with p300 and TP53 (PMID: 10518217). There is no evidence that it contacts DNA itself. Functions also in actin nucleation (PMID: 19287377). |
| JUP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KANSL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein is a component of the NSL chromatin remodelling complex |
| KAT2A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase |
| KAT2B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Interacts with TFs to modify histones (PMID: 9707565) |
| KAT5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone acetyltransferase |
| KAT6A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone deacetylase; likely a transcriptional cofactor |
| KAT6B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Co-factor. Could possibly bind to DNA, as a helix- turn-helix DNA-binding motif is present within its MYST-type HAT domain. |
| KAT8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBDs, no evidence of TF activity - looks like a chromatin protein. Included only because it has an x in Vaquerizas 2009. |
| KCNIP3 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
There are multiple papers showing DREAM can bind DNA (PMID: 10078534, PMID: 11108959). |
| KDM1A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Affects transcription by histone modification |
| KDM3A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Its a C6 zinc finger and Jumonji-type protein. No DBD. |
| KEAP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KIAA1549 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KIAA1683 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No evidence to support a DNA binding function |
| KIAA1958 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KIT |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KNTC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Rod_C domain localizes to kinetochores but has not been shown to be DNA-binding |
| KRAS |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KRBOX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
KRAB domain only - no DBD or evidence for independent DNA binding |
| KRTAP5-1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KRTAP5-9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| KRTAP9-9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Keratin-associated protein |
| LARP1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Classic RNA binding protein |
| LARP1B |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| LARP4 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Classic RNA binding protein |
| LARP4B |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Classic RNA binding protein |
| LARP6 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Classic RNA binding protein |
| LARP7 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Classic RNA binding protein |
| LGALS9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| LGR4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| LIG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA ligase. Binds DNA in the crystal structure (PDB: 1X9N) |
| LIG3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA ligase. Binds DNA in the crystal structure (PDB: 3L2P) |
| LMO2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Protein binds to bHLH TFs, which then bind to DNA (PMID: 9707419). Both transfac motifs are suspect - the bHLH motif likely resulted from an indirect interaction. |
| LMO4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| LPP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
znfLIM is probably not a DNA binding domain (PMID: 8506279). The protein has been reported to be coactivator for ETV4 (PMID: 16738319). |
| LRP5 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| LRP6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Cell surface receptor that is in the beginning of the WNT signaling cascade. GO annotation has no evidence of DNA-binding activity (PMID: 14739301). |
| LRP8 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| LRRFIP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Seems to be included only because GO catalogs positive regulation of NF-kappaB transcription factor activity. Nothing that would indicate DNA binding. |
| LRRFIP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Its paralog forms a complex with ETS1 that binds AGCCCCCGGCG sequences based on EMSA and SPR (PMID: 16199883). However, direct DNA binding by LRRFIP2 is not demonstrated, and it seems more likely that it is in the complex through protein-protein interactions. |
| LSR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Cell plasma membrane resident protein that functions in cell-cell junctions (PMID: 25753034) |
| LTF |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| LTN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| LZTFL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lactotransferrin - major iron-binding protein in milk. Two papers from the 1990s (PMID: 7854459; PMID: 1037119) demonstrate strong DNA binding. |
| LZTR1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| LZTS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contain a bZIP domain. (PMID: 10097140) does not examine TF activity or DNA binding - GO needs to be corrected. |
| MACC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MACF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because Vasquerizas 2009 includes it with an x. No DBD and no other data to support being a TF. |
| MAD2L2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Likely to be a DNA-binding protein that operates on DNA-repair (PMID: 25799990) |
| MALT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that operates upstream of NFKB in a signaling cascade (PMID: 18223652) |
| MAML1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
MAML1 does not contact the DNA in the structure (PDB: 2F8X), but contacts RBPJ, which in turn binds DNA |
| MAML3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAP2K5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase that operates upstream in the signaling cascade that leads to NFKB |
| MAP3K10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAP3K13 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAP3K7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a kinase |
| MAPK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
MAP kinase; protein array paper evidence is not strong |
| MAPK10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a kinase |
| MAPK11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAPK14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Well characterized MAPK. Included because it as a regulator of several TFs and GO captures this. |
| MAPK3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAPK8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MAPK9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MATR3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
An RBP that recognizes MAUCUUR-site based on Ray et al 2013 (PMID: 23846655) |
| MAVS |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates upstream in the signaling cascade that activates innate immunity response for viruses through NFLB and IRF3 TFs |
| MB21D1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA with backbone contacts and one minor groove inserting Arginine in the crystal structure (PDB: 4LEY) |
| MBTPS2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO annotation has no evidence of DNA-binding activity, only modulation of TF activity (PMID: 11163209) |
| MDFI |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
MDF1 is a co-repressor that inhibits DNA-binding (PMID: 8797820) |
| MDM2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| MDM4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein binds to, and inhibits, p53 (PMID: 9226370) |
| MED1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is a component of Mediator. |
| MED12 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED13 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED13L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED15 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED16 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is a component of Mediator. |
| MED17 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED21 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure of the yeast mediator complex (PDB: 5SVA) |
| MED23 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED24 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MED6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not bind anywhere near DNA on crystal structure (PDB: 4V1O) |
| MEN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Interacts with NFKB1 (PMID: 11526476), JUN, JUND, and ELK1 and represses their activities with a mechanism that is at least for JUN and JUND dependent on their phosphorylation |
| MET |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Its a cell surface receptor and kinase - included only because Vasquerizas 2009 included it with an x. |
| MGMT |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
O6-Alklyguanine-DNA alkyltransferase (AGT) is an important DNA repair protein that protects cells from mutagenesis and toxicity arising from alkylating agents (PMID: 15964013); structure (PDB: 1YFH) is with cytosine alkylated DNA |
| MID2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO citation (PMID: 23077300) has no evidence of DNA-binding activity |
| MINK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MKL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-factor |
| MKL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MKRN3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely E3 ubiquitin ligase. Contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs |
| MLLT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
X-ray structure indicates histone binding (PDB: 4TMP) |
| MLLT10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
No evidence showing MLLT10 can bind to DNA in a sequence-specific manner (PMID: 7888665) |
| MLLT11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MLLT3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcription elongation factor [PMID: 20159561; PMID: 20471948] |
| MLLT6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Likely to be a transcriptional cofactor based on presence of PHD domains and (PMID: 15588942) |
| MN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Evidence for DNA binding not strong in (PMID: 12569362) |
| MNAT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MPG |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA error repair enzyme that excises alkylation-damaged purine bases. Binds dsDNA in the crystal structure (PDB: 1BNK) |
| MRPL28 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because it has an X in Vaquerizas 2009 |
| MRRF |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MSH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA that has a base mismatch as a heterodimer with MSH6. Binds DNA in the crystal structure (PDB: 2O8B) |
| MSH3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in mismatch repair - binds dsDNA with indels (PDB: 3THZ) and changes DNA shape |
| MSH6 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA that has base mismatches as a heterodimer with MSH2. Binds DNA in the crystal structure (PDB: 2O8B) |
| MSL3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 3OA6). Contacts only the backbone and doesnt cause large changes in the DNA shape |
| MSRB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The paper cited by GO (PMID:10375640) called MSRB2 a TF based on amino acid sequence analysis, but did not provide any direct evidence |
| MST1R |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MTDH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MTF2 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Recent study (PMID: 28869966) demonstrates direct, specific DNA binding to CG-rich sequences through PBMs, and crystal structure in complex with DNA |
| MTPN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD; no evidence for DNA binding - only included because GO says its a positive regulator of NFkappaB. |
| MUS81 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
MUS81 is a structure-specific endonuclease subunit. It binds DNA in the crystal structure (PDB: 4P0P) in a heterodimeric complex with EME1. |
| MYBBP1A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Protein that activates TP53 (PMID: 24375404) and binds to MYB (PMID: 24375404); however, there is no evidence of direct binding to DNA |
| MYCBP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| MYD88 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates upstream in the signaling cascade (PMID: 22155231) |
| MYEF2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single-stranded DNA and can regulate transcription in transfection reporter assays |
| MYOCD |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor (PMID: 12640126) |
| NAB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Well characterized transcriptional co-repressor of e.g. EGR1 (PMID: 12427750) |
| NABP2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 4OWW) |
| NACC2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds DNA as a homodimer, recognizing a TGTCRSWWYYGWC consensus based on SELEX experiments (PMID: 22926524) |
| NCOA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NCOA5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known coactivator with no DBD |
| NCOA6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a transcriptional co-regulator (PMID: 10681503) |
| NCOA7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known co-activator; included only because TF-cat documents this |
| NDN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NDP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because GO says positive regulation of sequence-specific DNA binding transcription factor activity. Not DNA binding. |
| NEIL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA glycosylase 1. Binds DNA in the crystal structure (PDB: 5ITR) |
| NFAM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
NFAM1 modulates B cell signaling through its immunoreceptor tyrosine-based activation motif, which regulates B cell development (PMID: 15143214) |
| NFE4 |
Unknown |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
|
NFE4 does not posess a DBD. It is a member of the SSP complex that regulates B-globin gene expression, and binds DNA as a heteromer with CP2, based on EMSA (PMID: 7828600; PMID: 15273251). A shorter isoform prevents CP2 binding (PMID: 16263792) and is involved in repression. No gel-shift experiments have been performed in the absence of its partner, CP2, thus its likely an obligate heteromer. |
| NFKBIA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is I kappa B alpha, which interacts with NFkappaB. No DBD, and evidence indicates that it is not a TF. |
| NFKBIB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
From (PMID: 12686541), it appears that the ternary complex is stabilized by an interaction with this protein, which suggests that this protein may offer a conducive electrostatic environment rather directly contributing to the binding event. |
| NFKBID |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NFKBIL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NFKBIZ |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NFRKB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Has a winged helix but cannot bind to the NFKB consensus. |
| NFYB |
Unknown |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
|
Obligate heterotrimer of NFYA, NFYB, and NFYC |
| NFYC |
Unknown |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
PDB 4AWL is a very tightly intertwined heterotrimeric complex of NFYA, NFYB and NFYC with a plenty of protein-protein interactions. NFYA contains the recognition alpha-helix but there is no point considering any of the components separately as they are definitely complexed even in the solution and all contribute contacts with the DNA backbone. |
| NKRF |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds AATTTCCTCTGA based on EMSA (PMID: 11071890) and to AATTCCCTGA based on another EMSA (PMID: 16107696) |
| NLRC3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NLRC4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NLRC5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein inhibits NFKB activity |
| NLRP12 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NLRP2B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NLRP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates upstream in the signaling cascade |
| NME2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds to telomeres (PMID: 22135295). Binds specific sequences by gel-shift, and binding is impacted by a SNP (PMID: 23368879) |
| NOC3L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No evidence to support a DNA binding function |
| NOC4L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is associated with ribosome synthesis (PMID: 27798105) |
| NOCT |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Deadenylase protein that probably regulates genes post-transcriptionally (PMID: 22073225) |
| NOD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
NOD-proteins function in signaling cascades that report bacterial peptidoglycans. They activate kinases that in turn activate NFKB proteins etc. Reviewed in (PMID: 25526305) |
| NOD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NODAL |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a secreted signaling molecule |
| NONO |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RBP with RRM domains |
| NOP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| NOTCH1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
A transmembrane protein that inhibits MEF2C activation (PMID: 10082551). NOTCH1 does not bind DNA in the structure, and is not required for DNA binding, since RBPJ is bound without it in (PDB:4J2X). |
| NOTCH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transmembrane receptor protein that operates far upstream in the signaling cascade |
| NOTCH3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Fragment of NOTCH. Is a coactivator. |
| NPM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
No evidence for sequence-specific DNA-binding (PMID: 2223875) |
| NR0B2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcription cofactor - lacks a conventional DNA binding domain and represses the transcriptional activity of various nuclear receptors (PMID: 14752053) |
| NRF1 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NRG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Cell surface receptor - does not have predicted DBDs |
| NRIP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor |
| NRIP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Binds indirectly to DNA through interactions with NHR TFs (PMID: 10860982) |
| NRK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a kinase |
| NSD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a histone methyltransferase with H3K36 and H4K20 methylation activities (PMID: 12805229) |
| NTRK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Membrane bound receptor protein |
| NUCKS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a GRP core, which is similar to an AT-hook. But, the amino acids flanking the core are quite different from an AT-hook. Could non-specifically bind to DNA, but lacks compelling evidence. |
| NUP98 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| OGG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA error repairing enzyme. Binds DNA in the crystal structure (PDB: 1EBM), presumably without specificity |
| OPRD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transmembrane protein |
| OTOP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| OTULIN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PA2G4 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds CGGCAAAAAGG repeats based on EMSA performed with recombinant E.Coli expressed protein (PMID: 1507318) |
| PABPN1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| PARK7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates upstream in the signaling cascade |
| PARP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
|
DNA repair protein that binds dsDNA non-specifically (PMID: 21183686; PMID: 21262234). The Transfac motifs are likely NFAT target sites |
| PARP10 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Contains two RRM domains, so likely an RNA-binding protein. Myc-interacting factor capable of ADP-ribosylating itself and core histones (PMID: 15674325). |
| PAWR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that binds to several TFs such as PITX2 (PMID: 19801652) and appears to inactivate them |
| PAXBP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Has been shown to associate with PAX3 and PAX7, and recruits H3K4 methyltransferase complex (PMID: 22862948). Has a putative DNA-binding domain, so it could contribute to specificity or even function as an independent TF |
| PAXIP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional coactivator that associates with PAX2 (PMID: 10908331) |
| PCBD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Coactivator for HNF1A-dependent transcription. Regulates the dimerization of homeodomain protein HNF1A and enhances its transcriptional activity (UniProt: P61457) |
| PCBP1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Crystal structure shows it binds ssDNA (PDB: 1ZTG). |
| PCBP2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is an RBP. Structure (PDB:2PQU) is with single stranded DNA |
| PCBP3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
KH domain suggests that this is an RNA-binding protein |
| PCGF2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 8521824) shows via SELEX and EMSA that the recombinant PCGF2 protein binds GACT repeats |
| PCGF6 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds GACTNGACT based on SELEX and EMSA performed in (PMID: 8521824) |
| PCNA |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 5L7C). Protein barely contacts the DNA at all |
| PCSK6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PDCD7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD. No evidence for sequence-specific DNA binding. Included only because TFcat says its a cofactor. |
| PDS5B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| PELI1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Ubiquitin ligase |
| PER1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that associates with CLOCK-ARNTL heterodimers to silence the expression of their target genes (PMID: 16987893) |
| PER2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that operates in the circadian clock through binding to and inhibiting the ARNTL-CLOCK heterodimer. Does not bind DNA itself )PMID: 16987893) |
| PER3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PEX14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PFDN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PGBD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
PiggyBac Transposable Element Derived 1. Contains a SCAN domain and interacts with other SCAN proteins (see Q96JS3). Interpro also lists without ref that it has sequence specific DNA binding activity (IEA code). No concrete evidence available. |
| PGS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PHB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is likely a mitochondrial chaperone and thus its roles associated with transcription are likely to be very indirect (PMID: 10835343) |
| PHB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein has been shown to bind to TFs and function as a co-repressor. There appears to be no evidence for direct DNA-binding activity (PMID: 18629613) |
| PHF1 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Recent study (PMID: 28869966) demonstrates direct, specific DNA binding to CG-rich sequences through PBMs, and crystal structure in complex with DNA |
| PHF19 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Recent study (PMID: 28869966) demonstrates direct, specific DNA binding to CG-rich sequences of related proteins through PBMs, and crystal structure in complex with DNA |
| PHF5A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
This is a known spliceosomal protein with a PhD domain. I dont see the evidence that it binds the GJA1/Cx43 promoter, as listed on GeneCards. The reference cited does not mention this protein as far as I can see. In any case, binding could be indirect - the most likely role in transcription for a PHD domain protein would be as a cofactor. |
| PHTF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Despite its name, does not have a detectable Homeodomain. No available evidence for DNA binding. |
| PHTF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a Transcription factor homeodomain, male germ-cell domain (INTERPRO:IPR021980, PFAM:PF12129) that does not have any known DNA-binding activity. Its name comes from a fly ortholog that does contain a homeobox; but, the human gene does not. |
| PIAS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The protein contains a SAP motif, which has been annotated as a putative DNA-binding motif without supporting experimental evidence (PMID:10694879) |
| PIAS2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Sumoylates transcription factors to modulate their activities (PMID: 22406621; PMID: 15976810; PMID: 15920481) |
| PIAS3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
PIAS-proteins regulate transcription factors by sumoylating them (PMID: 12077349) |
| PIAS4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD. No evidence of DNA binding - its a known cofactor |
| PIDD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates upstream in the NFKB signaling cascade |
| PIKFYVE |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because its in Vasquerizas 2009 with an x. No DBD and no other evidence of DNA binding. |
| PIM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Affects transcription by phosphorylating TFs (PMID: 18593906) |
| PINK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PKHD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The TIG domain is potentially DNA-binding but there is no literature evidence to suggest that PKHD1 is a TF. Membrane protein that operates upstream in the signaling cascade leading to NFKB (PMID: 21300060) |
| PKHD1L1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Membrane receptor (PMID: 12620974) |
| PLA2G10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLA2G1B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLEK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The DEP-domain is a winged helix-turn-helix protein domain, and thus it is related to ETS, RFX, and FOX domains. However, there is no evidence for DNA-binding activity and it has been shown to operate in G-protein signalling upstream of TFs |
| PLEK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLEKHA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
No DBDs; no indication of DNA binding - included only because Vasquerizas 2009 included it with an x. |
| PLPP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLSCR1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
PLSCR1 has been demonstrated to bind a GTAACCATGTGGA sequence in the IP3R1 promoter (PMID:16091359), mediated by a specific portion of the protein. |
| PLXNA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PLXNA2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PLXNA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PLXNA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade (PMID: 12591607). |
| PLXNB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PLXNB2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLXNB3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PLXNC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PLXND1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a semaphorin receptor that operates far upstream on the signaling cascade. |
| PML |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely a transcriptional cofactor. Does not have any clear DBDs. RING-fingers are more typically protein-protein interaction domains |
| PNKP |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 3ZVN) |
| POGZ |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Has a potential DBD that is similar to Drosophila Brinker but no other data suggesting TF function. Likely co-factor. |
| POLA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4Q5V) |
| POLB |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase that participates in base excision repair. Binds DNA in the crystal structure (PDB: 1BPX) |
| POLE3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
|
| POLE4 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone-like subunit of DNA polymerase epsilon |
| POLG |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4ZTU) |
| POLH |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase. Binds DNA in the crystal structure (PDB: 3JAA) |
| POLI |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase. Binds DNA in the crystal structure (PDB: 1T3N) |
| POLK |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase. Binds DNA in the crystal structure (PDB: 2OH2) |
| POLL |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase. Binds DNA in the crystal structure (PDB: 1RZT) |
| POLM |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase that operates on non-homologous end joining. Binds DNA in the crystal structure (PDB: 2IHM) |
| POLN |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4XVI) |
| POLQ |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4X0P) |
| POLR1B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
General Transcription Factor |
| POLR2A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contacts DNA in the structure (PDB: 5FLM) |
| POLR2B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Contacts DNA in the structure (PDB: 5FLM) |
| POLR2E |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
RNA-polymerase subunit. Binds DNA in the crystal structure (PDB: 5IY6) |
| POLR2J |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FLM) |
| POLR2K |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FLM) |
| POLR2L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FLM) |
| POLR3A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Transfac motifs are dubious, and do not appear to be similar to any known motifs. |
| POLRMT |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 4BOC) |
| POT1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 1XJV) |
| POU2AF1 |
Unknown |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Requires POU2F1 to bind DNA. In the crystal structure (PDB:1CQT), POU2AF1 contacts both the POU2F1 and DNA major groove |
| PPARGC1A |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| PPARGC1B |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Contains a single RRM domain, so could possibly be an RNA binding protein |
| PPP1R13L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PPP2R3B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PPP2R5B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PPP3CA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PPRC1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| PQBP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Has a WW domain. May interact with Pol II, but no indication of sequence specific DNA binding |
| PRAM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRAP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRB3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Human salivary glycoprotein |
| PRDM7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Only has KRAB and SET domains - no C2H2 ZFs. |
| PRDX3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PREB |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
In vitro gel-shift experiments show that PREB binds specific promoter sequences (PMID: 10194769; PMID: 19426980) without the presence of a canonical DBD |
| PREX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because Vasquerizas 2009 includes it with an x. No DBD and no other data to support being a TF. |
| PREX2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRIM2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds DNA-RNA hybrid in the structure (PDB: 5F0Q) |
| PRIMPOL |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in DNA replication. Binds DNA in the crystal structure (PDB: 5L2X), presumably non-specifically. |
| PRKCB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRKCH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a kinase that activates another kinase leading to degradation of NFKB inhibitor NFKBIA (PMID: 21820409) |
| PRKCI |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase that operates upstream in the signaling cascade that leads to NFKB |
| PRKCQ |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRKCZ |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRKD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRKD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRKN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiquitin ligase |
| PRMT2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PRNP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PSMA6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PSMC5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PSMD10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO annotation has no evidence of DNA-binding activity; only modulation of NF-kappaB activity (PMID: 18040287) |
| PSMD11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PSMD12 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PSPC1 |
Unknown |
No |
ssDNA/RNA binding |
3 Low specificity DNA-binding protein |
No motif |
|
Contains RRMs and no DBDs. Mouse orhtolog has been found in androgen receptor complexes (PMID: 16641145) but no DNA-binding activity has been shown. |
| PTCH1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PTEN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PTGIS |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
It is a cytochrome p450 enzyme |
| PTH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PTTG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO annotation has no evidence for DNA-binding activity (PMID:9811450), only transcriptional activation in reporter experiments |
| PUM3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds dsDNA in the crystal structure (PDB: 4WZW). Makes extensive contacts with the backbone that cause shape changes and could possibly lead to specificity. |
| PURA |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds dsDNA (PMID: 15282343) and ssDNA (PMID: 1448097) specifically |
| PURB |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds dsDNA (PMID: 15282343) and ssDNA (PMID: 1448097) specifically |
| PURG |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Paralogs PURA and PURB bind dsDNA (PMID: 15282343) and ssDNA (PMID: 1448097) specifically. |
| PYCARD |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PYDC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| PYDC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that regulates NFKB activity |
| QRICH1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RAB7B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein activates NFKB (PMID: 20953574) |
| RAD21 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Motifs are suspicious; protein is a component of the cohesin complex and there is no evidence for direct binding to DNA. |
| RAD51 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Functions in homologous recombination DNA-repair. Binds DNA with low specificity (PMID:10390347) |
| RAG1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds DNA specifically (PMID: 10066757) |
| RAI1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Chromatin remodeler |
| RAPGEF3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD and no evidence its a TF - included only because it has an x in Vaquerizas 2009 |
| RAPGEF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RAPGEF5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Classic co-factor |
| RBBP7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RBCK1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Fairly well-studied E3 ubiquitin-protein ligase. But EMSA data exist demonstrating binding to TGG-containing DNA (PMID: 9514928) |
| RBL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RBL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-repressor |
| RBM10 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein |
| RBM20 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely an RNA-binding protein |
| RBM22 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA binding protein (PMID: 17045351) |
| RBM26 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein (PMID: 22681889; PMID: 22658674) |
| RBM27 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely an RNA-binding protein |
| RBM5 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein that binds RNA with two RRM-domains and regulates splicing (PMID: 24486491) |
| RBM6 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein that binds RNA with two RRM-domains and regulates splicing (PMID: 24332178) |
| RCAN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
SH3 domain protein that interacts with calcineurin. GO annotation and abstract in (PMID: 8595418) appear erroneous - mentions a binding domain in the abstract, but no evidence is provided in the paper. |
| RECQL |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
ATP dependent DNA helicase. Binds DNA in the crystal structure (PDB: 2WWY) |
| RELL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RELN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a large secreted extracellular matrix protein |
| REV1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA polymerase. Binds DNA in the crystal structure (PDB: 3GQC) |
| REXO4 |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
REXO4 (hPMC2) has been shown to bind ERE containing sequences in gel-shift experiments (PMID: 10908561) in complex with ERbeta. However, figures containing the gel-shifts have been cropped to exclude the unshifted free DNA band so it is hard to judge the evidence. |
| RFC1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA-dependent ATPase. Binds DNA (contact with major groove and backbone) in the crystal structure (PDB: 2K7F) |
| RFXANK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
AKA RFX-B. No DBD, no motifs produced when tested, no evidence of independent DNA binding. (PMID: 9806546) shows that its interaction with RFX5 and RFXAP is essential for binding of the RFX complex to MHC-II promoters, but it does not bind DNA on its own. |
| RFXAP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included because TF-CAT calls it a cofactor and GO erroneously calls it sequence-specific DNA binding. |
| RGCC |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RGS11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| RGS6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RGS7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RGS9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RHEBL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RING1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
RING1 is a well-characterized member of the Polycomb complex. No reference to DNA-binding in literature search on EntrezGene |
| RIOK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RIPK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RIPK2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein activates NFKB through its kinase activity |
| RIPK3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase protein |
| RIPK4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RLIM |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
LIM ZF proteins are unlikely to bind DNA |
| RNASE2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RNASEH1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Ribonuclease H1. Binds DNA-RNA hybrid in structure (PDB: 2QKB) |
| RNF114 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RNF125 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiguitin ligase |
| RNF138 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
DNA repair protein. RNF138 is recruited to DNA damage sites through zinc fingers that have a strong preference for DNA with 5- or 3-single-stranded overhangs. (PMID: 26502055) |
| RNF14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor |
| RNF166 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiquitin ligase (PMID: 26456228) |
| RNF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Forms non-specific DNA contacts according to crystal structure (PMID: 25355358) |
| RNF25 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Probably a co-regulator; no clear evidence for direct binding to DNA |
| RNF31 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RNF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiquitin ligase (PMID: 18408734) |
| RNF41 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiquitin ligase |
| RPA2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RPA4 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
ssDNA binding protein involved in DNA repair (PMID: 7760808) |
| RPL7 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA by filter binding (PMID: 8441630), but competition assays suggest it is non-specific. A specific dsRNA structure is thought to be the preferred substrate. RNA-binding has been demonstrated by gel-shift experiments (PMID: 10329420). |
| RPL7A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RPS27A |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| RPS6KA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RPS6KA5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD - its a kinase. Included only because GO says its an upstream regulator of CREB and NF-kappaB |
| RRN3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RUNX1T1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| RWDD3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included because GO says negative regulation of NF-kappaB transcription factor activity. No DBD, no motif, etc |
| RYBP |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Contains RanBP ZFs, so likely an RNA-binding protein |
| S100A12 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| S100A8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| S100A9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SAFB |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Based on this review the protein is likely to bind AT-rich DNA in a non-sequence specific manner (PMID: 27888239) |
| SAFB2 |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Bind AT-rich DNA elements and RNA (PMID: 27888239) |
| SAV1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SCAND1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SCAND2P |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
|
| SCAPER |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Involved in cell cycle regulation in the cytoplasm (PMID: 17698606) |
| SCMH1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Has a SLED domain (IPR021987). (PMID: 24727478) claims, based on NMR, that SLED is a sequence-specific DBD with relatively high specificity |
| SCML1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Homologous to polycomb proteins, so likely a transcriptional cofactor (PMID: 9570953). Has putative roles in the testis development and spermatogenesis (PMID:18601738). Reference cited by GO provides no evidence of DNA-binding activity (PMID: 9570953). |
| SCML2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Part of the polycomb repressor complex that functions in male, establishing the male germline epigenome through regulation of histone H2A ubiquitination (PMID: 25703348) |
| SEMA4A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SERTAD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-factor; no evidence for DNA-binding activity |
| SERTAD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor that associates with E2F/TFDP heterodimers (PMID: 19152710). Does not contain any DBDs |
| SETD6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Methyltransferase to the NF-kappaB complex (PMID: 21131967) and histones (PMID: 23324626) |
| SF3A2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Functions in splicing |
| SF3A3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
RNA-binding protein |
| SFPQ |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Splicing factor - contains 2 RRM domains |
| SFRP4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SFRP5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SFTPB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SGK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SGK3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein kinase that operates upstream in the signaling cascade |
| SHH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SHPRH |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SIGIRR |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SIK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SIN3A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Motifs are suspect and probably reflect DNA binding specificities of SIN3 contacted TFs. SIN3 does not have any DBDs and is thought to function as a scaffold protein that connects TFs to HDAC complexes. Reviewed in (PMID: 19505602) |
| SIN3B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Can be tethered to DNA by Mad-Max, but does not appear to have any specificity (PMID: 7889570) |
| SIRT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SIRT2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SIRT3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a histone de-acetylase |
| SIRT6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
No canonical DBD, but it does bind at least one sequence-specific DNA binding protein (TRF2). Seems more likely to be a cofactor. |
| SIVA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Affects transcription through interactions with NF-kappaB (PMID: 16491128) |
| SKI |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Conflicting evidence. Binds specifically to GTCTAGAC via EMSA in one study (PMID: 9452486). But, needs to form complexes with other proteins, such as NFI, to bind to DNA in another (PMID: 9380514). Related to SKIL, which also has evidence for DNA binding (PMID: 9824161) |
| SKIDA1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SKIL |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Homodimerizes on GTCTAGAC sequence (EMSA) (PMID: 9824161) |
| SKOR1 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SLC22A4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a transmembrane protein of the plasmamembrane |
| SLC26A10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SLC26A3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included as a candidate only because GO cites a 1993 paper where sequence analysis identified a homeodomain. But, there seems to be no homeodomain. |
| SLC30A9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SLC39A10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SLC4A10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SMARCA2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
No clear DBD, and its a known cofactor |
| SMARCA4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
(PMID: 24752179) shows via ChIP that it has DNA mediated regulatory activity, but unknown if this is direct or indirect binding. No clear DBD present in the protein. |
| SMARCAL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Is a DNA binding helicase |
| SMARCB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Alias INI1 is a minor groove DNA-binding protein (PMID: 19398554) |
| SMARCD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
It is an active ATP-utilizing chromatin remodeling protein (PMID: 25818293) |
| SMARCD2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Transcriptional cofactor (PMID: 8804307) |
| SMARCD3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Chromatin remodelling complex component |
| SMC3 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds and compacts DNA as a SMC1-SMC3 heterodimer that is part of the cohesin complex (PMID: 23620281). Transfac motifs likely reflect the binding of other TFs such as CTCF that associate with cohesin |
| SMO |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The protein is a G-protein coupled receptor |
| SMUG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in DNA mismatch repair. Xenopus homolog binds dsDNA in the crystal structure (PDB: 1OE4) |
| SMYD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SMYD3 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds GGAGGG elements based on SELEX performed using GST fusion protein (PMID: 15235609) |
| SNAPC2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Recognizes the PSE-element, which is located in the core promoters of snRNA genes, and helps to recruit TBP (PMID: 8633057) |
| SNAPC5 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds specifically to the PSE (PMID: 9732265) |
| SNRPC |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Component of the spliceosomal U1 snRNP |
| SNURF |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely a TF co-factor |
| SNW1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SOGA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contain any likely DBDs. |
| SON |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
The protein has been reported to bind a GAKANSRCC consensus based on SELEX experiments. Recognizes a matching GAGACCACC sequence in a hepatitis B virus regulatory element (PMID: 11306577) |
| SORBS2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SPEN |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
Has a putative AT-hook |
Data inconclusive. Contains RRM domains, suggesting RNA binding activity. Gel-shift experiments demonstrate that SPEN (aka MINT) binds ss and dsDNA G- and T-rich elements (PMID: 10451362), but in another system SPEN does not bind DNA directly and is recruited (PMID: 15778499). RNA-binding activities have also been documented (PMID: 24748666). |
| SPHK1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SPZ1 |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds to E-boxes (EMSA) (PMID: 15226296) |
| SSB |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds to the 3 poly(U) terminus of nascent RNA polymerase III transcripts, protecting them from exonuclease digestion and facilitating their folding and maturation (PMID: 3192525; PMID: 2470590] |
| SSBP2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in DNA damage response. Has domain IPR008116 Sequence-specific single-strand DNA-binding protein |
| SSBP3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Single stranded DNA binding protein. There is no evidence for sequence specificity, although it can operate as a transcriptional co-regulator (PMID: 26495868) |
| SSBP4 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
(PMID:9531483) shows that the SSDP_DNA-bd domain has sequence-specific single-stranded DNA-binding activity. |
| SSH1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SSH2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SSH3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SSX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| STAG1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Part of the cohesin complex |
| STK16 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| STK3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Kinase - included only because GO says it regulates TFs |
| STK36 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| STRN |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| STRN3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GO annotation has no evidence for DNA-binding activity (PMID: 11570823), and STRN3 lacks a canonical DBD |
| SUB1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
The structure (PDB: 2C62) demonstrates binding to single stranded DNA |
| SUFU |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SUMO1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| SUPT16H |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Component of the FACT histone remodeling complex, which functions in transcriptional elongation (PMID: 12934006). (PDB: 4Z2M) shows that the protein contacts H3 and H4 proteins, but it could also contact DNA |
| SUPT4H1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Involved in transcription elongation (PMID: 9450929) |
| SUPT5H |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein that regulates transcriptional elongation (PMID: 9450929) |
| SUPT6H |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
SPT6 is an elongation factor, not a TF. GO needs to be corrected - (PMID: 8786132) does not demonstrate sequence specificity or DNA binding. |
| SUV39H1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a histone methyltransferase that trimethylates lysine 9 of histone H3 |
| SUV39H2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Histone (H3K9) methyltransferase. Also directs DNA methylation (UniProt: Q9H5I1) (PMID: 14765126) |
| SUZ12 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein is a component of the PRC2 repressor complex, which silences DNA through histone methylation. The protein has two znf C2H2-like domains that appear to be used in association with chromatin (PMID: 24100017) |
| SYK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known co-factor |
| TAB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TAB2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Works as a protein-protein interaction adapter to recruit TAK1-kinase (PMID: 10882101). Could also work as an RBP, based on presence of a zf-RanBP domain |
| TAB3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| TADA3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Paper cited by GO annotation has no evidence of specific DNA-binding activity (PMID: 9674425), and is based on experiments using an entire complex |
| TAF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Contacts DNA in the structure (PDB: 5FUR). Transfac motifs are suspect, and are probably in vivo signals derived from promoter binding TFs (e.g. YY1 and ETS) |
| TAF10 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
General transcription factor |
| TAF11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not interact with DNA (PMID: 15657423) |
| TAF12 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
(PMID: 15601843) shows it has DNA binding activity in a complex with TAF4b. |
| TAF13 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Forms heterodimer TAF11:TAF13, which has a histone-fold like structure and could thus bind DNA in a non- or low specific manner (PMID: 9695952) |
| TAF1A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
General TF. Directly binds to DNA, likely in a non sequence-specific manner (PMID: 15970593), although it is possible it might have some specificity. |
| TAF1B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Pol I TAF that contacts the rDNA promoter in conjunction with TBP and UBF (PMID: 7491500). No clear evidence that it directly confers sequence specificity. |
| TAF1C |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Component of the transcription factor SL1/TIF-IB complex, which is involved in the assembly of the PIC. |
| TAF1L |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in preinitiation complex assembly (general transcriptional machinery. Is a paralog of TAF1, which binds DNA based on the structure (PDB: 5FUR) |
| TAF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Directly contact with DNA in TFIID complex (PMID: 27096372), and mediate major interactions with the downstream promoter together with TAF1. Contacts DNA in the structure (PDB: 5FUR) |
| TAF3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contacts chromatin through modified histones and TFs such as TP53 (PMID: 18549481) |
| TAF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
The TAF4 domain interacts with TAF12 and makes a novel histone-like heterodimer that binds DNA and has a core promoter function for of a subset of genes (PMID: 19635797; PMID: 12237304) |
| TAF4B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Histone-like protein that binds DNA as an obligate heterodimeric complex with TAF12 (PMID: 19635797). Target sequence needs to be over 70 bases long and doesnt appear to have sequence specificity |
| TAF5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TAF5L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Paralog of TAF5 that is unlikely to contact DNA (PMID: 17227857) |
| TAF6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FUR) |
| TAF6L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Part of the PCAF Histone Acetylase Complex (PMID: 9674425). Structurally similar to TAF6, which does not contact DNA directly |
| TAF7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FUR) |
| TAF7L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TAF8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contact DNA in the structure (PDB: 5FUR) |
| TAF9 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Related to histone H3. (PMID: 15601843) shows DNA binding activity in complex with TAF4b, but does not demonstrate intrinsic sequence specificity. May contact promoter DNA (PMID: 23292512) |
| TAF9B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TARDBP |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Is an RNA-binding protein that can also bind single stranded DNA, as in the structure (PDB: 3D2W) |
| TAX1BP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TBL1Y |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD. Included as a candidate only because TFcat lists it as a putative coactivator. |
| TCEA2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely binds RNA based on similarity to TCEA1 |
| TCEAL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TCEAL7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Modulates transcription, but there is no evidence for DNA binding (PMID: 19966855) |
| TCEAL8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lacks a canonical DBD |
| TCF19 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Previous evidence (PMID: 1868030) for TF activity is based on sequence analysis (high proline content), and presence of an FHA domain. However, neither prove ability to bind DNA in a sequence-specific manner |
| TCF20 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 7760812) identified this protein in a library screen and demonstrated DNA binding of an IVT product to an enhancer of interest. They also identified a putative bZIP domain that is not detected by Pfam or SMART. (PMID:10995766) subsequently mapped the strongest DNA binding site. |
| TCF25 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Only evidence is based on (PMID:16574069), which claims that hnulp1 (TCF25) contains a possible bHLH domain and that it represses transcription in a Gal4-forced recruitment assay. |
| TDG |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
TDG is specific for G/T mispairs in DNA (PDB: 2RBA; PMID: 18587051). Some evidence exists for TDG affecting transcription through interactions with NHR TFs (PMID: 9694815), suggesting it could also be a transcriptional co-factor |
| TDP1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 1NOP) |
| TDP2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds single stranded DNA in the structure (PDB: 4F1H) |
| TET2 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Binds DNA in the crystal structure (PDB: 4NM6). Oxidizes 5-methylcytosine (5mC). |
| TGFB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TGFB1I1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Available evidence suggests that it acts as a co-factor |
| TGS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is an RNA-modifying enzyme (PMID: 19307714) |
| THRAP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| THYN1 |
Unknown |
Yes |
Likely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure (PDB: 5J3E). Recognizes 5mC containing DNA. Contacts the DNA backbone from the side of the minor groove and has an arginine that inserts into the minor groove. |
| TIA1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Has an RRM domain. Binds single stranded DNA in the structure (PDB: 5ITH) |
| TICAM1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TIPARP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TIRAP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TLE1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-factor |
| TLE2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TLE3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Protein is a transcriptional co-regulator (PMID: 21459326) |
| TLE4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
TLE4 is a Groucho protein (co-repressor) |
| TLE6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional cofactor that associates with FOXG1 (PMID: 16314515) |
| TLR2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Upstream of NFKB and not involved in DNA-binding |
| TLR3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Binds dsRNA (PMID: 16111635) |
| TLR4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TLR9 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Protein is a nonmethylated CpG dsDNA recognizing protein that operates in the innate immune response to pathogen invasion of the cell. It isnt a TF, but it binds pathogenic DNA (PMID: 11564765). Binds single-stranded DNA in the structure (PDB: 3WPC) |
| TMEM235 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transmembrane protein |
| TMF1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Bacterially-expressed protein binds specifically to the TATA element to compete with TBP, based on EMSA (PMID: 1409643) |
| TNF |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
The protein is a secreted cytokine and operates far upstream in the signaling cascade |
| TNFAIP3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Inhibits NFKB-activation. No evidence for direct binding to DNA |
| TNFRSF11A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TNFRSF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates far upstream in the signaling cascade |
| TNFSF11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TNFSF18 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a cytokine |
| TNFSF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Extracellular signaling molecule. Included only because it regulates TFs. |
| TONSL |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds to the N-terminal tail of Histone H4 (PMID: 27338793, PDB: 5JA4). It is likely a histone chaperone (PMID: 26527279) and thus probably forms nonspecific contacts with DNA. |
| TOP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA topoisomerase. Binds DNA in the crystal structure (PDB: 1A31). |
| TOP2A |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA topoisomerase. Binds DNA in the crystal structure (PDB: 4FM9). |
| TOP2B |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
DNA topoisomerase. Binds DNA in the crystal structure (PDB: 3QX3). |
| TOPORS |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| TP53BP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
|
| TRADD |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Regulates transcription by binding to the adaptor protein TRAF2, leading to reduction of recruitment of inhibitor-of-apoptosis proteins. No evidence for binding DNA (PMID: 18309324) |
| TRAF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
TRAF1 is an NF-kappaB interactor (PMID: 10692572), and is unlikely to have DNA-binding activity |
| TRAF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Does not contain any canonical DBDs |
| TRAF3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRAF4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates far upstream in the signaling cascade |
| TRAF5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates far upstream in the signaling cascade |
| TRAF6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRAPPC9 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TREX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Has weak exonuclease activity for GAG, ACA, and CTGC DNA sequences (PMID: 17355961) |
| TRIB1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Associates with CEBPB and CEBPA and inhibits their activities (PMID: 17724128). This is probably achieved through control of their proteosomal degradation (PMID: 17576771) |
| TRIB3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Disabled kinase - binds NFkappaB and ATF4, but no evidence for direct sequence specific DNA binding. |
| TRIM13 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Operates far upstream in the signaling cascade. Ring fingers usually operate in protein-protein interactions |
| TRIM14 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM15 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM21 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM22 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM23 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM24 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Known cofactor. Included because TF-CAT documents this. Does not have any canonical DBDs. |
| TRIM25 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM26 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM27 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Evidence presented in (PMID: 1437549) for DNA-binding of alias RFP is not strong - if anything, this is likely a non-specific DNA binder |
| TRIM28 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
This protein a well-known co-repressor and is recruited to DNA by KRAB-domain containing TFs. Transfac motifs are likely from interacting proteins |
| TRIM29 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Previous evidence for TF activity (PMID: 8188213) is based on sequence analysis and does not provide DNA-binding evidence. Based on EntrezGene information, its likely a transcriptional co-factor |
| TRIM3 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Contains multiple NHL domains, which bind RNA (see, for example, LRP8). |
| TRIM31 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM32 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM33 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM34 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM37 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Included only because GO says it is a regulator of NFkappaB. No evidence for DNA binding, and no canonical DBD. |
| TRIM38 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIM40 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein that promotes post-translational modification of an NBKB-inhibitor protein (PMID: 21474709) |
| TRIM5 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBD and no evidence for DNA binding. Included as a candidate only because GO says its a regulator. |
| TRIM52 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Established ubiquitin ligase that targets at least one viral protein (NS2A) of Japanese Encephalitis Virus to proteosomal degradation (PMID: 27667714) |
| TRIM62 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ubiguitin ligase (PMID: 23402750) |
| TRIM8 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRIP11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Structural component of the Golgi-apparatus (PMID: 19112494) |
| TRIT1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Protein is a tRNA modifying enzyme (PMID: 15870694) |
| TRMT1L |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TRRAP |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a component of histone acetyltransferase complexes |
| TSC2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TSC22D1 |
Unknown |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
TSC22D1 appears to homo- and heterodimerize with other TFs to affect transcription (PMID: 10488076). In vitro, it has been shown to bind GC-rich DNA sequences (PMID: 9022669) |
| TSC22D2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
There is some evidence that a related protein (TSC22D1) binds DNA specifically - thus, it is possible this is also a TF. |
| TSC22D3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
There is some evidence that a related protein (TSC22D1) binds DNA specifically - thus, it is possible this is also a TF. |
| TSC22D4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
There is some evidence that a related protein (TSC22D1) binds DNA specifically - thus, it is possible this is also a TF. |
| TSN |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Based on (PMID: 20450889) and (PMID: 12484770), this protein binds repetitive DNA sequences as multimeric complexes that may contain partner protein TSNAX |
| TSSK4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| TUB |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
The Tubby C-terminal domain (IPR000007; PF01167) has been shown to impart nuclear localization and bind select dsDNA sequences in gel-shift experiments (PMID: 10591637). This article hypothesized that this domain constitutes a bona fide sequence specific TF, but no concrete evidence for this exists to date |
| TULP4 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
(PMID: 10591637) shows that it binds dsDNA. All other research, however, supports phosphoinositide-binding as the major function of the tubby domain. |
| TUT1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
|
| TXK |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Experimental evidence for DNA-binding was performed with nuclear extract - thus, the apparent specific-binding of TXK could be due to indirect binding (PMID: 11859127). In addition a whitepaper suggests that this interaction could not be replicated (Miskimins, Beth) |
| U2AF1 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Well-established RNA binding protein |
| U2AF1L4 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Related to U2AF1, so likely also an RNA binding protein. |
| UBA52 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBB |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBC |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBE2K |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBE2N |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBE2V1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Ubiquitin ligase |
| UBN1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Interacts with bZIP transcription factors (PMID: 10725330) |
| UBR4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UBTFL6 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
According to ENSEMBL this is a Pseudogene, and it is of uncertain confidence in Uniprot. The most similar gene, UBTLF1, is annotated as No evidence for or against specific DNA-binding by this class of HMG box containing proteins. |
| UFL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UHRF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Structural evidence (PDB:2ZO0; PDB: 2ZO1; PMID: 18772888] and (PDB: 2ZKE) (PMID: 18772891) demonstrate direct DNA-binding. However, the extent to which it is sequence specific beyond hemimethylated DNA has not been extensively explored. |
| UHRF2 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds DNA in the crystal structure contacting the minor groove and backbone (PDB: 4PW5). Recognizes 5hmC-containing DNA (PDB: 4PW5) |
| UNG |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Involved in mismatch repair. Excises uracil bases from DNA. Binds DNA in the crystal structure (PDB: 1EMJ) |
| USP39 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| USP7 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| UTF1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| VAV1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Paper cited by GO annotation (PMID: 2477241) only presents evidence based on sequence similarity to a ZF motif, and other evidence (PMID: 11994417) only supports a role in coactivation of NFAT and NFKB without direct DNA-binding |
| VEGFA |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Extracellular signaling molecule. Included only because it regulates CREB. |
| VGLL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Likely transcriptional cofactor (PMID: 10518497) |
| VGLL2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Co-activator that binds TEF family TFs (PMID: 14762206) |
| VGLL3 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 23380592) describes this protein as a co-activator, and it doesnt seem to have a DBD (fig. 1) |
| VHLL |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Interacts with TFs as part of an E3 ubiquitin ligase complex (PMID: 12682018). No evidence for DNA binding. |
| VPS72 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
VPS72 (YL1) is a histone chaperone. YL1 binding to the H2A.Z-H2B dimer is mutually exclusive from the dimer binding DNA (PMID: 26974126) |
| WFS1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| WNT1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| WNT10B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a secreted signaling protein |
| WNT2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| WNT3A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| WNT5A |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
(PMID: 19847889) shows this protein as a part of a large EMSA shifting complex with RNA-Pol1, CHD1, and other DNA binding proteins. It does not, however, show evidence for it binding to DNA directly |
| WNT8B |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
WNT family signaling molecule (PMID: 9536085) |
| WRN |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
ATP dependent DNA helicase. Binds DNA in the crystal structure (PDB: 3AAF) |
| WWOX |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Co-factor of AP-2 (PMID: 15548692) |
| WWP2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| WWTR1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Transcriptional co-activator that binds to TEADs (PMID: 19324877) and TBX5 (PMID: 16332960) |
| XCL1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a secreted chemokine |
| XPA |
Unknown |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Functions in DNA repair (PMID: 19197159), but has a strong HT-SELEX-derived motif. |
| YEATS2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| YEATS4 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Lacks a DBD and the study cited by GO annotation (PMID: 9302258) doesnt have experimental evidence for DNA-binding |
| YOD1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ZBED6CL |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
No DBDs on UniProt or Ensembl |
| ZBP1 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
ZBP1 is structurally-specific for Z-DNA, but does not have any sequence specificity (PDB: 1J75; PMID: 11524677) |
| ZCCHC11 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely a ssDNA or RNA binding protein based on domain composition |
| ZCCHC6 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
(PMID: 23709223) shows that it binds single-stranded nucleid acids |
| ZDHHC11 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
|
| ZDHHC19 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
ER transmembrane protein |
| ZMAT2 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Possibly an RBP based on presence of a U1 ZF domain |
| ZNF137P |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Pseudogene |
Pseudogene |
| ZNF185 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Protein has a LIM-subtype ZF. This type of ZF is not likely to bind DNA (PMID: 17696879) |
| ZNF638 |
Unknown |
No |
Unlikely to be sequence specific TF |
3 Low specificity DNA-binding protein |
No motif |
|
Binds C-rich dsDNA with low affinity (PMID: 8647861). |
| ZNF720 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a KRAB domain (associated with many C2H2 ZFs), but no annotated C2H2 on PDB or UniProt |
| ZNF738 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Contains a KRAB domain (associated with many C2H2 ZFs), but no annotated C2H2 on PDB or UniProt |
| ZNF862 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Has a putative AT-hook |
Contains a KRAB domain (associated with many C2H2 ZFs), but no annotated C2H2 on PDB or UniProt |
| ZNFX1 |
Unknown |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Probably an RBP (PMID: 22658674; PMID: 22681889) |
| ZRANB2 |
Unknown |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Its the wrong kind of zinc finger to bind DNA. Likely binds RNA. PMID cited by GO (PMID: 9931435) does not have evidence of sequence-specific DNA binding. |
| TP53 |
p53 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| TP63 |
p53 |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TP73 |
p53 |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| PAX1 |
Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX5 |
Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX8 |
Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PAX9 |
Paired box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LCOR |
Pipsqueak |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| LCORL |
Pipsqueak |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PROX1 |
Prospero |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| PROX2 |
Prospero |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFAT5 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFATC1 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFATC2 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFATC3 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFATC4 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFKB1 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFKB2 |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| REL |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| RELA |
Rel |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Can bind as a homodimer or heterodimer (PMID: 22101729) |
| RELB |
Rel |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Likely an obligate heteromer (PMID: 22101729) |
| RFX1 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX2 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX3 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX4 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX5 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
|
| RFX6 |
RFX |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX7 |
RFX |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RFX8 |
RFX |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
RFX8 has the HUGO-approved name RFX family member 8, lacking RFX DNA binding domain?.? I cannot find the original evidence, however, and RFX8 clearly encodes a complete and high-confidence RFX DNA binding domain.? So, it seems more likely than not to be DNA binding (TRH) |
| RUNX1 |
Runt |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| RUNX2 |
Runt |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| RUNX3 |
Runt |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| AIRE |
SAND |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Binds to TTATTA and tandem repeats of ATTGGTTA (PMID: 11533054) |
| DEAF1 |
SAND |
Yes |
Inferred motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| GLA |
SAND |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
GLA appears to lack a functional SAND domain. It encodes a well-characterized enzyme, Galactosidase Alpha. Most of the polypeptide encodes a glycoside hydrolase domain and most of the rest encodes another pfam domain called Glycoside hydrolase family 27. It has a low-scoring SAND domain match that almost certainly overlaps with a known domain related to its function as an enzyme. |
| GMEB1 |
SAND |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| GMEB2 |
SAND |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SKOR2 |
SAND |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SP100 |
SAND |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Gel-shift experiments using human SP100 have shown binding to specific TTCG half sites (PMID: 11427895). |
| SP110 |
SAND |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SP140 |
SAND |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SP140L |
SAND |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| SART1 |
SART-1 |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
Likely an RNA-binding protein |
| RPL36A |
SBP |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Protein is a ribosomal component |
| NFIA |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFIB |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFIC |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| NFIX |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SMAD1 |
SMAD |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Well-established obligate heteromer |
| SMAD2 |
SMAD |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
A 30 amino-acid insertion encoded by exon 3 is thought to displace the hairpin loop, providing a structural explanation for SMAD2s lack of DNA-binding activity (PMID: 11532220). |
| SMAD3 |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SMAD4 |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
|
| SMAD5 |
SMAD |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| SMAD6 |
SMAD |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
In the inhibitory Smads, Smad6 and Smad7 and DAD, the MH1 domains are replaced by divergent amino-termini that share regions of similarity within the inhibitory Smad subgroup (PMID: 11532220). |
| SMAD7 |
SMAD |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
In the inhibitory Smads, Smad6 and Smad7 and DAD, the MH1 domains are replaced by divergent amino-termini that share regions of similarity within the inhibitory Smad subgroup (PMID: 11532220). |
| SMAD9 |
SMAD |
Yes |
Known motif |
2 Obligate heteromer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| STAT1 |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| STAT2 |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| STAT3 |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| STAT4 |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| STAT5A |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| STAT5B |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
Can form both homodimers and heterodimers with STAT5A (PMID: 9528750) |
| STAT6 |
STAT |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
Only known motifs are from Transfac or HocoMoco - origin is uncertain |
|
| EOMES |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| MGA |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
Has a putative AT-hook |
Some isoforms also contain a predicted bHLH domain, but it is unlike any other known bHLH domain and the MGA motif looks like a standard T-box motif, so the bHLH domain is likely a false positive |
| T |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBR1 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX1 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX10 |
T-box |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX15 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX18 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX19 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX2 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX20 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX21 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX22 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
|
| TBX3 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX4 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
Available motifs suggest facultative homodimeric binding |
| TBX5 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBX6 |
T-box |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TBP |
TBP |
Yes |
Known motif |
1 Monomer or homomultimer |
100 perc ID - in vitro |
|
Binds DNA in the pre-initiation complex |
| TBPL1 |
TBP |
Yes |
Likely to be sequence specific TF |
2 Obligate heteromer |
No motif |
|
A more distant paralog of TBP and the only member of the TBP family that lacks the ability to bind the TATA box. (PMID: 21711503). In vitro, purified TLF-TFIIA binds directly to the NF1 promoter (PMID: 15767669), so likely an obligate heteromer. |
| TBPL2 |
TBP |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| LIN54 |
TCR/CxC |
Yes |
Inferred motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
In the structure (PDB: 5FD3), the protein contacts DNA, although it only contacts the backbone except for one tyrosine residue |
| TESMIN |
TCR/CxC |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
Has a double CxC DBD structure. One is eroded, and it did not produce a motif on PBMs. So, either it has lost its ability to bind DNA, or the experiment failed for some reason. |
| APOA4 |
TEA |
No |
Unlikely to be sequence specific TF |
4 Not a DNA binding protein |
No motif |
|
APOA4 is Apolipoprotein A4. It consists entirely of Apolipoprotein A1/A4/E domains. The protein product is excluded from the nucleus. I cant see that it has a TEA domain. I believe it is likely to be a low-scoring domain match that almost certainly overlaps with a known domain related to its function as an enzyme. Thus it is unlikely to be a DNA binding protein. |
| TEAD1 |
TEA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TEAD2 |
TEA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TEAD3 |
TEA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| TEAD4 |
TEA |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| THAP1 |
THAP finger |
Yes |
Known motif |
1 Monomer or homomultimer |
In vivo/Misc source |
|
Likely binds as a homodimer |
| THAP10 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Paralog THAP1 binds DNA in a sequence specific manner |
| THAP11 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
(PMID: 26876175) has a ChIP-seq motif with GGGARWTGTAGT consensus. THAP11 is an atypical zinc-finger paralogous to THAP1, which has a crystal structure (PDB: 2KO0) where the protein contacts bases TGGGCA |
| THAP12 |
THAP finger |
Yes |
Known motif |
1 Monomer or homomultimer |
High-throughput in vitro |
|
|
| THAP2 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP3 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP4 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP5 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP6 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP7 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP8 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
|
| THAP9 |
THAP finger |
Yes |
Likely to be sequence specific TF |
1 Monomer or homomultimer |
No motif |
|
Human THAP9 Gene Encodes an Active P-Element DNA Transposase (PMID: 23349291) |
| ZFAND5 |
ZZ-type ZF |
No |
ssDNA/RNA binding |
4 Not a DNA binding protein |
No motif |
|
An RNA-binding protein that recognises 3UTR located AU-rich elements in mRNA molecules to stabilize them (PMID: 22665488) |