| HGNC approved symbol | HGNC ID | HGNC approved name | Entrez gene ID | UniProt AC (human) | UniProt ID (human) | Pfam domains | MGI symbol | MGI ID | UniProt AC (mouse) | UniProt ID (mouse) | HGNC gene family tag | HGNC gene family description | Function | Modification | PMID for information on function | Protein complex | Target molecule | Target entity | Product | PMID for information on target | Comment | Status of entry |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AIRE
(details) |
360 | autoimmune regulator | 326 | O43918 | AIRE_HUMAN | HSR PF03172 5-102, SAND PF01342 200-239, PHD PF00628 299-340 | Aire | 1338803 | Q9Z0E3 | AIRE_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification read, TF | # | 18292755 | # | histone, DNA | H3K4, H3K4me3, DNA motif | # | 18292755 | AIRE selectively interacts with histone H3 through its first plant homeodomain (PHD) finger (AIRE–PHD1) and preferentially binds to non-methylated H3K4 (H3K4me0). Accordingly, in vivo AIRE binds to and activates promoters containing low levels of H3K4me3 in human embryonic kidney 293 cells. AIRE–PHD1 is an important member of a newly identified class of PHD fingers that specifically recognize H3K4me0, thus providing a new link between the status of histone modifications. | # |
|
APOBEC3H
(details) |
24100 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3H | 164668 | Q6NTF7 | ABC3H_HUMAN | APOBEC3 PF18771 25-157 | # | # | # | # | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 22001110 | APOB_mRNA_editosome | DNA, RNA | ssDNA, mRNA, mC | dhU | 22001110 | Fig. A2 in the reference (Targets are exogenous retroviruses ssDNA like HIV or transposable elements/ endogenous retroelements e.g. LINEs, SINEs and LTR). | # |
|
ARNTL
(details) |
701 | aryl hydrocarbon receptor nuclear translocator-like | 406 | O00327 | BMAL1_HUMAN | HLH PF00010 74-126, PAS PF00989 149-254, PAS_11 PF14598 339-442 | Arntl | 1096381 | Q9WTL8 | BMAL1_MOUSE | bHLH | Basic helix-loop-helix proteins | Histone modification write cofactor, TF | TF activator | 14645221, 24395244 | # | histone | # | # | 14645221, 24395244 | The coincidence of a rhythm in histone H3 and histone H4 acetylation on the proximal E-box of hPer1 with transcriptional activation of per1 and per2 is consistent with the heterodimeric complexes of CLOCK, NPAS2 and BMAL1 = ARNTL recruiting a histone acetyltransferase (HAT)-containing transcriptional co-activation complex to achieve maximal target gene activation; CLOCK:BMAL1 functions like pioneer transcription factors and regulates the DNA accessibility of other transcription factors. | # |
|
ATF2
(details) |
784 | activating transcription factor 2 | 1386 | P15336 | ATF2_HUMAN | bZIP_1 PF00170 354-411 | Atf2 | 109349 | P16951 | ATF2_MOUSE | bZIP | Basic leucine zipper proteins | Histone modification write, TF | Histone acetylation, TF activator | 10821277 | # | histone, DNA | H2B, H4, DNA motif | # | 10821277 | ATF-2 is a histone acetyltransferase (HAT), which specifically acetylates histones H2B and H4 in vitro, exhibits histone acetyltransferase (HAT) activity. | # |
|
ATF7IP
(details) |
20092 | activating transcription factor 7 interacting protein | 55729 | Q6VMQ6 | MCAF1_HUMAN | ATF7IP_BD PF16788 570-783, fn3_4 PF16794 1160-1259 | Atf7ip | 1858965 | Q7TT18 | MCAF1_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 14536086 | # | histone | # | # | 14536086 | Promoter H3-K9 trimethylation is the cause of transcriptional repression and that mAM/hAM facilitates conversion of H3-K9 dimethyl to trimethyl by ESET/SETDB1. | # |
|
ATXN7
(details) |
10560 | ataxin 7 | 6314 | O15265 | ATX7_HUMAN | SCA7 PF08313 332-395 | Atxn7 | 2179277 | Q8R4I1 | ATX7_MOUSE | ATXN | Ataxins | Histone modification write cofactor | Histone acetylation | 16494529 | SAGA | histone | # | # | 16494529 | Ataxin-7 (ATXN7) is a subunit of the GCN5 histone acetyltransferase–containing coactivator complexes TFTC/STAGA. TFTC/STAGA complexes purified from SCA7 mice have normal TRRAP, GCN5, TAF12, and SPT3 levels and that their histone or nucleosomal acetylation activities are unaffected. | # |
|
ATXN7L3
(details) |
25416 | ataxin 7-like 3 | 56970 | Q14CW9 | AT7L3_HUMAN | Sgf11 PF08209 81-112, SCA7 PF08313 207-237 | Atxn7l3 | 3036270 | A2AWT3 | AT7L3_MOUSE | # | # | Histone modification erase cofactor | Histone deubiquitination | 18206972 | SAGA | histone | # | # | 18206972 | ATXN7L3, USP22, and ENY2 are the human orthologs of yeast Sgf11, Ubp8, and Sus1, respectively, and they are integral components of TFTC/STAGA complex. These three proteins together form a module of the TFTC/STAGA complex, which specifically removes the ubiquitin moiety from monoubiquitinated histones H2A and H2B. | # |
|
BARD1
(details) |
952 | BRCA1 associated RING domain 1 | 580 | Q99728 | BARD1_HUMAN | zf-RING_6 PF14835 42-107, Ank_2 PF12796 428-523, BRCT PF00533 569-643 | Bard1 | 1328361 | O70445 | BARD1_MOUSE | ANKRD | Ankyrin repeat domain containing | Histone modification write | Histone ubiquitination | 19916563 | BRCC, BRCA1-A | histone | H2AX, H2A, H2B, H3, H4 | H2AXub, H2Aub, H2Bub, H3ub, H4ub | 19916563, 12485996 | BARD1, like CstF-50, also interacts with RNA polymerase II. BARD1-mediated inhibition of polyadenylation may prevent inappropriate RNA processing during transcription, | # |
|
BAZ1B
(details) |
961 | bromodomain adjacent to zinc finger domain, 1B | 9031 | Q9UIG0 | BAZ1B_HUMAN | WAC_Acf1_DNA_bd PF10537 22-121, WHIM1 PF15612 726-762, WSD PF15613 899-1026, PHD PF00628 1187-1231, Bromodomain PF00439 1348-1427 | Baz1b | 1353499 | Q9Z277 | BAZ1B_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification write | Histone phosphorylation | 19092802 | B-WICH, WINAC | histone | H2AXT142, H3 | H2AXY142ph | 19092802 | WSTF=BAZ1B phosphorylates Tyr 142 of H2A.X, and WSTF activity has an important role in regulating several events that are critical for the DNA damage response. | # |
|
BPTF
(details) |
3581 | bromodomain PHD finger transcription factor | 2186 | Q12830 | BPTF_HUMAN | DDT PF02791 241-299, PHD PF00628 393-434 2870-2915, WSD PF15613 457-524, Bromodomain PF00439 2939-3018 | Bptf | 2444008 | # | # | PHF | Zinc fingers, PHD-type | Chromatin remodeling | # | 18974875 | NuRF | chromatin | # | # | 18974875 | Chromatin remodeling protein Bptf (Bromodomain PHD-finger Transcription Factor), the largest subunit of NURF (Nucleosome Remodeling Factor) in a mammal. | # |
|
BRCA1
(details) |
1100 | breast cancer 1, early onset | 672 | P38398 | BRCA1_HUMAN | zf-C3HC4 PF00097 24-64, BRCT_assoc PF12820 361-492, BRCT PF00533 1649-1724 1758-1845 | Brca1 | 104537 | P48754 | BRCA1_MOUSE | RNF, PPP1R | RING-type (C3HC4) zinc fingers, Serine/threonine phosphatases / Protein phosphatase 1, regulatory subunits | Histone modification write cofactor, TF | Histone acetylation, Histone methylation, Histone ubiquitination, TF activator, TF repressor | 20820192 | BRCC, BRCA1-A | DNA | DNA motif | # | 20820192 | BRCA1 acts as a transcription factor, which regulates expression of many genes involved in many biological processes. DNMT1, the methylation maintenance enzyme, is a transcriptional target of BRCA1. Impaired function of BRCA1 leads to global DNA hypomethylation, loss of genomic imprinting, and an open chromatin configuration in several types of tissues examined in a BRCA1 mutant mouse model at premaligant stages. BRCA1 deficiency is also associated with significantly increased expression levels of several protooncogenes. | # |
|
CDK7
(details) |
1778 | cyclin-dependent kinase 7 | 1022 | P50613 | CDK7_HUMAN | Pkinase PF00069 12-295 | Cdk7 | 102956 | Q03147 | CDK7_MOUSE | CDK, TFIIH | Cyclin-dependent kinases, General transcription factor IIH complex subunits | Histone modification write | Histone phosphorylation | 10722743 | # | histone | H1 | # | 10722743 | Cdk7, is able to phosphorylate histone H1, and the basal activity is increased 2-fold in the presence of recombinant human cyclin H (the activating partner of Cdk7). | # |
|
CTCF
(details) |
13723 | CCCTC-binding factor (zinc finger protein) | 10664 | P49711 | CTCF_HUMAN | zf-C2H2 PF00096 266-288 294-316 322-345 351-373 379-401 437-460 555-575 | Ctcf | 109447 | Q61164 | CTCF_MOUSE | ZNF | Zinc fingers, C2H2-type | Chromatin remodeling, TF | TF activator | 16949368 | # | DNA | DNA motif | # | 16949368 | A CTCF-CHD8 complex is involved in both enhancer blocking and epigenetic remodeling at chromatin boundary in vivo. | # |
|
CXXC1
(details) |
24343 | CXXC finger protein 1 | 30827 | Q9P0U4 | CXXC1_HUMAN | PHD PF00628 29-73, zf-CXXC PF02008 163-208, CpG_bind_C PF12269 400-636 | Cxxc1 | 1921572 | Q9CWW7 | CXXC1_MOUSE | PHF | Zinc fingers, PHD-type | Chromatin remodeling, TF | # | 21407193 | COMPASS | DNA | CG, DNA motif | # | 21407193 | CFP1=CXXC1 is a CXXC domain-containing protein. CXXC domain proteins direct different chromatin-modifying activities to various chromatin regions. | # |
|
E2F6
(details) |
3120 | E2F transcription factor 6 | 1876 | O75461 | E2F6_HUMAN | E2F_TDP PF02319 65-128, E2F_CC-MB PF16421 143-237 | E2f6 | 1354159 | O54917 | E2F6_MOUSE | # | # | TF | TF repressor | # | RING2-L3MBTL2, CHD8, MLL2/3, MLL4/WBP7 | DNA | DNA motif | # | # | Epigenetic complex (MLL) partner. | # |
|
ENY2
(details) |
24449 | enhancer of yellow 2 homolog (Drosophila) | 56943 | Q9NPA8 | ENY2_HUMAN | EnY2 PF10163 13-95 | Eny2 | 1919286 | Q9JIX0 | ENY2_MOUSE | # | # | Histone modification erase cofactor | Histone ubiquitination | 18206972 | SAGA | histone | # | # | 18206972 | ATXN7L3, USP22, and ENY2 are required as cofactors for the full transcriptional activity by nuclear receptors. Thus, the deubiquitinase activity of the TFTC/STAGA HAT complex is necessary to counteract heterochromatin silencing and acts as a positive cofactor for activation by nuclear receptors in vivo. | # |
|
FAM175A
(details) |
25829 | family with sequence similarity 175, member A | 84142 | Q6UWZ7 | F175A_HUMAN | MPN_2A_DUB_like PF21125 9-172 | Fam175a | 1917931 | Q8BPZ8 | F175A_MOUSE | # | # | Scaffold protein | # | 19261749 | BRCA1-A | TF | # | # | 19261749 | Abra1=FAM175A protein, which appears to act as a scaffold for the A complex. Abra1 is known to mediate the interaction of Rap80 with BRCA1. | # |
|
FOXA1
(details) |
5021 | forkhead box A1 | 3169 | P55317 | FOXA1_HUMAN | Forkhead_N PF08430 16-169, Forkhead PF00250 170-255, HNF_C PF09354 396-455 | Foxa1 | 1347472 | P35582 | FOXA1_MOUSE | FOX | Forkhead boxes | Chromatin remodeling, TF | # | 22406422 | # | chromatin, DNA | DNA motif | # | # | FOXA1 functions in organizing nucleosome positioning. | # |
|
FOXO1
(details) |
3819 | forkhead box O1 | 2308 | Q12778 | FOXO1_HUMAN | Forkhead PF00250 160-244, FOXO_KIX_bdg PF16675 430-506, FOXO-TAD PF16676 597-635 | Foxo1 | 1890077 | Q9R1E0 | FOXO1_MOUSE | FOX | Forkhead boxes | TF | # | 22406422 | # | histone, DNA | DNA motif, H3, H4 | # | # | FOXO1 interacts with core histones H3 and H4. | # |
|
FOXP1
(details) |
3823 | forkhead box P1 | 27086 | Q9H334 | FOXP1_HUMAN | FOXP-CC PF16159 302-370, Forkhead PF00250 465-541 | Foxp1 | 1914004 | P58462 | FOXP1_MOUSE | FOX | Forkhead boxes | TF | # | 22406422 | # | histone, DNA | DNA motif | # | # | Recruitment of specific chromatin-modifying complexes with HDAC activity. | # |
|
FOXP2
(details) |
13875 | forkhead box P2 | 93986 | O15409 | FOXP2_HUMAN | FOXP-CC PF16159 342-410, Forkhead PF00250 504-581 | Foxp2 | 2148705 | P58463 | FOXP2_MOUSE | FOX | Forkhead boxes | TF | # | 22406422 | # | histone, DNA | DNA motif | # | # | Recruitment of specific chromatin-modifying complexes with HDAC activity. | # |
|
FOXP3
(details) |
6106 | forkhead box P3 | 50943 | Q9BZS1 | FOXP3_HUMAN | FOXP-CC PF16159 193-263, Forkhead PF00250 337-414 | Foxp3 | 1891436 | Q99JB6 | FOXP3_MOUSE | FOX | Forkhead boxes | TF | # | 22406422 | # | histone, DNA | DNA motif | # | # | Recruitment of specific chromatin-modifying complexes with HDAC activity. | # |
|
FOXP4
(details) |
20842 | forkhead box P4 | 116113 | Q8IVH2 | FOXP4_HUMAN | FOXP-CC PF16159 305-371, Forkhead PF00250 467-544 | Foxp4 | 1921373 | Q9DBY0 | FOXP4_MOUSE | FOX | Forkhead boxes | TF | # | 22406422 | # | histone, DNA | DNA motif | # | # | Recruitment of specific chromatin-modifying complexes with HDAC activity. | # |
|
GSG2
(details) |
19682 | germ cell associated 2 (haspin) | 83903 | Q8TF76 | HASP_HUMAN | Haspin_kinase PF12330 420-783 | Gsg2 | 1194498 | Q9Z0R0 | HASP_MOUSE | # | # | Histone modification write | Histone phosphorylation | 20705812 | # | histone | H3T3 | H3T3ph | 20705812 | Phosphorylation of histone H3 threonine 3 (H3T3ph) by Haspin=GSG2 is necessary for CPC accumulation at centromeres and that CPC subunit Survivin binds directly to H3T3ph. | # |
|
GTF2I
(details) |
4659 | general transcription factor IIi | 2969 | P78347 | GTF2I_HUMAN | GTF2I PF02946 112-188 360-436 465-541 569-647 733-809 868-942 | Gtf2i | 1202722 | Q9ESZ8 | GTF2I_MOUSE | # | # | TF | # | 9334314 | BHC | DNA | DNA motif | # | # | Added because it is a complex partner. | # |
|
GTF3C4
(details) |
4667 | general transcription factor IIIC, polypeptide 4, 90kDa | 9329 | Q9UKN8 | TF3C4_HUMAN | TFIIIC_delta PF12657 61-517, DUF5921 PF19336 516-592, zf-TFIIIC PF12660 741-789 | Gtf3c4 | 2138937 | Q8BMQ2 | TF3C4_MOUSE | KAT, GTF | Chromatin-modifying enzymes / K-acetyltransferases, General transcription factors | Histone modification write | Histone acetylation | 10523658 | # | histone | H3 | # | 10523658 | hTFIIIC90=GTF3C4 has an intrinsic histone acetyltransferase activity with a substrate specificity for histone H3. | # |
|
HDGF
(details) |
4856 | hepatoma-derived growth factor | 3068 | P51858 | HDGF_HUMAN | PWWP PF00855 13-93 | Hdgf | 1194494 | P51859 | HDGF_MOUSE | # | # | Chromatin remodeling, TF | TF repressor | 18331345, 17974029 | # | DNA | DNA motif | # | 18331345 | SUMOylated HDGF is not bound to chromatin. | # |
|
HINFP
(details) |
17850 | histone H4 transcription factor | 25988 | Q9BQA5 | HINFP_HUMAN | zf-C2H2_4 PF13894 229-251, zf-C2H2 PF00096 255-278 345-368 | Hinfp | 2429620 | Q8K1K9 | HINFP_MOUSE | ZNF | Zinc fingers, C2H2-type | Histone modification read, TF | TF activator, TF repressor | 14585971 | # | histone, DNA | H4, DNA motif | # | 14585971 | HiNF-P interacts with conserved H4 cell cycle regulatory sequences in vivo. | # |
|
HLTF
(details) |
11099 | helicase-like transcription factor | 6596 | Q14527 | HLTF_HUMAN | HIRAN PF08797 61-154, SNF2-rel_dom PF00176 242-720, zf-C3HC4_2 PF13923 760-800, Helicase_C PF00271 834-950 | Hltf | 1196437 | Q6PCN7 | HLTF_MOUSE | RNF | RING-type (C3HC4) zinc fingers | Chromatin remodeling cofactor | # | 18719106 | # | chromatin | # | # | 18719106 | Acts as a ubiquitin ligase for 'Lys-63'-linked polyubiquitination of chromatin-bound PCNA. | # |
|
IKZF1
(details) |
13176 | IKAROS family zinc finger 1 (Ikaros) | 10320 | Q13422 | IKZF1_HUMAN | zf-C2H2 PF00096 145-167 173-195 201-224 | Ikzf1 | 1342540 | Q03267 | IKZF1_MOUSE | ZNF, IKZF | Zinc fingers, C2H2-type, IKAROS zinc fingers | Chromatin remodeling, TF | # | 19141594 | # | DNA | DNA motif | # | 19141594 | Ikaros=IKZF1 forms dimers and multimers efficiently, and it has been proposed that Ikaros induces heterochromatization or chromatin remodeling of mouse DNA, resulting in repression or activation of target genes. The results provide insight into possible structural and functional roles of pericentromeric regions in mouse and human chromosomes. | # |
|
IKZF3
(details) |
13178 | IKAROS family zinc finger 3 (Aiolos) | 22806 | Q9UKT9 | IKZF3_HUMAN | zf-C2H2 PF00096 146-168 202-222 | Ikzf3 | 1342542 | O08900 | IKZF3_MOUSE | ZNF, IKZF | Zinc fingers, C2H2-type, "IKAROS zinc fingers" | TF | # | # | # | DNA | DNA motif | # | # | Associates with histone deacetylase complexes containing HDAC1, MTA2 and SIN3A. (UniProt) | # |
|
KAT2A
(details) |
4201 | K(lysine) acetyltransferase 2A | 2648 | Q92830 | KAT2A_HUMAN | PCAF_N PF06466 92-335, Acetyltransf_1 PF00583 536-627, Bromodomain PF00439 738-819 | Kat2a | 1343101 | Q9JHD2 | KAT2A_MOUSE | KAT | Chromatin-modifying enzymes / K-acetyltransferases | Histone modification write | Histone acetylation | 10611234 | TFTC-HAT, SAGA, ATAC, STAGA | histone | # | # | 10611234 | Current models of HAT protein activity suggest that one hypothesis for the role of hGCN5=KAT2A in c-Myc's activities might be due to the relaxing of chromatin packaging at target genes following histone acetylation by hGCN5. | # |
|
KLF18
(details) |
51793 | Kruppel like factor 18 | 105378952 | A0A0U1RQI7 | KLF18_HUMAN | zf-C2H2 PF00096 994-1018 1024-1046 | Zfp352 | 2387418 | A2AML7 | A2AML7_MOUSE | KLF | Kruppel like factors | TF | # | 24244731 | # | DNA | DNA | # | 24244731 | # | New |
|
MAX
(details) |
6913 | MYC associated factor X | 4149 | P61244 | MAX_HUMAN | HLH PF00010 24-74 | Max | 96921 | P28574 | MAX_MOUSE | bHLH | Basic helix-loop-helix proteins | Histone modification write cofactor, TF | Histone methylation, Histone acetylation, TF activator, TF repressor | 18271930, 12004135 | CHD8, MLL2/3, MLL4/WBP7 | DNA | DNA motif | # | 18271930, 12004135 | Part of a multimeric protein complex that contains E2F6, Mga and Max. The complex contains chromatin modifiers such as a novel histone methyltransferase that modifies lysine 9 of histone H3, HP1gamma, and Polycomb group (PcG) proteins. | # |
|
MBD1
(details) |
6916 | methyl-CpG binding domain protein 1 | 4152 | Q9UIS9 | MBD1_HUMAN | MBD PF01429 2-70, zf-CXXC PF02008 169-215 219-262 331-377 | Mbd1 | 1333811 | Q9Z2E2 | MBD1_MOUSE | # | # | Histone modification write cofactor, TF | Histone methylation, TF repressor | 15327775 | # | DNA | mCG, DNA motif | # | 15327775 | MBD1 recruits SETDB1 to the large subunit of chromatin assembly factor CAF-1 to form an S phase-specific CAF-1/MBD1/SETDB1 complex that facilitates methylation of H3-K9 during replication-coupled chromatin assembly. In the absence of MBD1, H3-K9 methylation is lost at multiple genomic loci and results in activation of p53BP2 gene, normally repressed by MBD1 in HeLa cells. Data suggest a model in which H3-K9 methylation by SETDB1 is dependent on MBD1 and is heritably maintained through DNA replication to support the formation of stable heterochromatin at methylated DNA. | # |
|
MBD2
(details) |
6917 | methyl-CpG binding domain protein 2 | 8932 | Q9UBB5 | MBD2_HUMAN | MBD PF01429 150-213, MBDa PF16564 221-294, MBD_C PF14048 296-385 | Mbd2 | 1333813 | Q9Z2E1 | MBD2_MOUSE | # | # | Histone modification write cofactor, Histone modification erase cofactor, TF | Histone methylation, Histone acetylation, TF repressor | 16415179 | NuRD, MeCP1 | DNA | mCG, DNA motif | # | 16415179 | Wild-type subnuclear distribution of p66alpha and p66beta depends on the presence of MBD2. Both proteins interact with the tails of all octamer histones in vitro, and acetylation of histone tails interferes with p66 binding. | # |
|
MBIP
(details) |
20427 | MAP3K12 binding inhibitory protein 1 | 51562 | Q9NS73 | MBIP1_HUMAN | Mbip | 1918320 | Q99LQ1 | MBIP1_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 19103755 | ATAC | histone | # | # | 19103755 | Novel proteins identified as STAGA/ TFTC subunits, such as ATAC2, DR1, MBIP, WDR5, YEATS2, and ZZZ3/ATAC1. | # | |
|
MECP2
(details) |
6990 | methyl CpG binding protein 2 | 4204 | P51608 | MECP2_HUMAN | MBD PF01429 97-159 | Mecp2 | 99918 | Q9Z2D6 | MECP2_MOUSE | # | # | Histone modification write cofactor, Histone modification write cofactor, TF | Histone methylation, Histone acetylation, TF repressor | 10773092 | # | DNA | mCG, DNA motif | # | 10773092 | Methyl-CpG-binding protein 2 (MeCP2) contains a transcriptional repression domain (TRD), which can act by recruitment of a large transcriptional co-repressor complex containing histone deacetylases HDAC1 and 2. | # |
|
MGA
(details) |
14010 | MGA, MAX dimerization protein | 23269 | Q8IWI9 | MGAP_HUMAN | T-box PF00907 77-259, MGA_dom PF16059 1043-1085, HLH PF00010 2425-2474 | Mga | 1352483 | A2AWL7 | MGAP_MOUSE | # | # | Histone modification write cofactor, TF | Histone methylation, Histone acetylation, TF activator, TF repressor | # | RING2-L3MBTL2, CHD8, MLL2/3, MLL4/WBP7 | DNA | DNA motif | # | # | Added because it is a complex partner | # |
|
MTF2
(details) |
29535 | metal response element binding transcription factor 2 | 22823 | Q9Y483 | MTF2_HUMAN | Tudor_2 PF18104 49-84, PHD PF00628 105-154, Mtf2_C PF14061 544-590 | Mtf2 | 105050 | Q02395 | MTF2_MOUSE | TDRD, PHF | Tudor domain containing, "Zinc fingers, PHD-type" | Polycomb group (PcG) protein | # | 21881606 | PRC2 | histone | H3K36me3 | # | 21881606 | Polycomb group (PcG) that binds histone H3 trimethylated at Lys-36. | # |
|
MYBBP1A
(details) |
7546 | MYB binding protein (P160) 1a | 10514 | Q9BQG0 | MBB1A_HUMAN | DNA_pol_phi PF04931 38-834 | Mybbp1a | 106181 | Q7TPV4 | MBB1A_MOUSE | # | # | Chromatin remodeling cofactor | # | 16603771 | B-WICH | chromatin | # | # | 16603771 | The WSTF (Williams syndrome transcription factor) protein is involved in vitamin D-mediated transcription and replication as a component of two distinct ATP-dependent chromatin remodeling complexes, WINAC and WICH, respectively. The WICH complex (WSTF-SNF2h) interacts with several nuclear proteins as follows: Sf3b155/SAP155, RNA helicase II/Guα, Myb-binding protein 1a, CSB. | # |
|
MYO1C
(details) |
7597 | myosin IC | 4641 | O00159 | MYO1C_HUMAN | Myosin_head PF00063 49-718, IQ PF00612 737-755 758-778, Myosin_TH1 PF06017 887-1058 | Myo1c | 106612 | Q9WTI7 | MYO1C_MOUSE | MYOI | Myosins / Myosin superfamily : Class I | Chromatin remodeling cofactor | # | 16603771 | B-WICH | chromatin | # | # | 16603771 | The WSTF (Williams syndrome transcription factor) protein is involved in vitamin D-mediated transcription and replication as a component of two distinct ATP-dependent chromatin remodeling complexes, WINAC and WICH, respectively. The WICH complex (WSTF-SNF2h) interacts with several nuclear proteins as follows: Sf3b155/SAP155, RNA helicase II/Gualpha, Myb-binding protein 1a, CSB, the proto-oncogene Dek, and nuclear myosin 1 in a large 3-MDa assembly, B-WICH, during active transcription. | # |
|
NAA60
(details) |
25875 | N(alpha)-acetyltransferase 60, NatF catalytic subunit | 79903 | Q9H7X0 | NAA60_HUMAN | Acetyltransf_1 PF00583 27-155 | Naa60 | 1922013 | Q9DBU2 | NAA60_MOUSE | NAA | N(alpha)-acetyltransferase subunits | Histone modification write | Histone acetylation | 21981917 | # | histone | H4K20, H4K79, H4K91 | H4K20ac, H4K79ac, H4K91ac | 21981917 | HAT4 =NAA60 is localized in the Golgi apparatus and displays a substrate preference for lysine residues of free histone H4, including H4K79 and H4K91, that reside in the globular domain of H4. | # |
|
NFRKB
(details) |
7802 | nuclear factor related to kappaB binding protein | 4798 | Q6P4R8 | NFRKB_HUMAN | NFRKB_winged PF14465 375-480 | Nfrkb | 2442410 | Q6PIJ4 | NFRKB_MOUSE | INO80 | INO80 complex subunits | Chromatin remodeling cofactor, TF | # | 16230350 | Ino80 | DNA | DNA motif | # | 16230350 | Five proteins appear to be unique to the human INO80 complex. NFRKB is a large (more than 1300 amino acids) protein. The C-terminal half of NFRKB contains low complexity, mucin-like repeats. | # |
|
NFYB
(details) |
7805 | nuclear transcription factor Y, beta | 4801 | P25208 | NFYB_HUMAN | CBFD_NFYB_HMF PF00808 58-122 | Nfyb | 97317 | P63139 | NFYB_MOUSE | # | # | Chromatin remodeling, TF | TF activator | 15243141, 23332751 | # | DNA | DNA motif | # | 23332751 | NF-Y is a sequence-specific transcription factor with nucleosome-like properties of nonspecific DNA binding and helps establish permissive chromatin modifications at CCAAT promoters. | # |
|
NOC2L
(details) |
24517 | nucleolar complex associated 2 homolog (S. cerevisiae) | 26155 | Q9Y3T9 | NOC2L_HUMAN | Noc2 PF03715 331-624 | Noc2l | 1931051 | Q9WV70 | NOC2L_MOUSE | # | # | Chromatin remodeling, TF | TF repressor | 15100215 | # | histone | H3 | # | 15100215 | INHAT =NOC2L (inhibitor of acetyltransferases) is a specific histone H3 N-terminal tail-binding complex. | # |
|
NPAS2
(details) |
7895 | neuronal PAS domain protein 2 | 4862 | Q99743 | NPAS2_HUMAN | HLH PF00010 11-58, PAS PF00989 84-151, PAS_11 PF14598 250-353 | Npas2 | 109232 | P97460 | NPAS2_MOUSE | bHLH | Basic helix-loop-helix proteins | Chromatin remodeling, TF | TF activator | 14645221, 24196956 | # | DNA | DNA motif | # | 14645221 | There is a time-dependent recruitment of chromatin remodeling machinery by NPAS2 in vivo. | # |
|
PHF1
(details) |
8919 | PHD finger protein 1 | 5252 | O43189 | PHF1_HUMAN | Tudor_2 PF18104 34-69, PHD PF00628 90-139, Mtf2_C PF14061 534-564 | Phf1 | 98647 | Q9Z1B8 | PHF1_MOUSE | TDRD, PHF | Tudor domain containing, Zinc fingers, PHD-type | Polycomb group (PcG) protein | # | 18086877 | PRC2 | # | # | # | 18086877 | The EED-EZH2 complex, containing the core subunits EZH2, EED, SUZ12, and RbAp48, functions as a histone H3K27-specific methyltransferase. The related EED-EZH2 protein complex is distinguished from the previous complex by the presence of another PcG protein, hPHF1. | # |
|
PHF19
(details) |
24566 | PHD finger protein 19 | 26147 | Q5T6S3 | PHF19_HUMAN | Tudor_2 PF18104 43-78, PHD PF00628 99-148, Mtf2_C PF14061 531-578 | Phf19 | 1921266 | Q9CXG9 | PHF19_MOUSE | TDRD, PHF | Tudor domain containing, Zinc fingers, PHD-type | Chromatin remodeling, Histone modification write cofactor | Histone acetylation | 15563832 | PRC2 | histone | # | # | 15563832 | Based on motifs identified within the hPCL3 =PHF19 open reading frames, hPCL3 proteins are likely to be nuclear proteins that regulate transcription and/or chromatin structure. | # |
|
PRDM16
(details) |
14000 | PR domain containing 16 | 63976 | Q9HAZ2 | PRD16_HUMAN | PRDM2_PR PF21549 84-212, zf-C2H2_6 PF13912 230-250, zf-C2H2 PF00096 281-303 309-331 337-360 366-388 394-416 424-443 951-973 979-1002 1008-1030 | Prdm16 | 1917923 | A2A935 | PRD16_MOUSE | ZNF | Zinc fingers, C2H2-type | Histone modification write cofactor, TF | Histone methylation, TF repressor | 12816872, 23856557 | # | histone, DNA | H3K9, DNA motif | H3K9me | 23856557 | The Prdm family may possess HKMTase properties. Some Prdms show intrinsic HKMTase activity (Prdm2, Prdm3, Prdm8, Prdm9, and Prdm16). In addition, Prdm1, Prdm5, and Prdm6 lack intrinsic HKMTase activity, but instead recruit G9a/Ehmt2/KMT1C, a strong mammalian histone H3 lysine 9 (H3K9) methyltransferase, to mediate HKMTase activity (see Fog et al., 2012 for a review). Another structural feature is that the Prdm family has multiple kruppel-type zinc finger (ZF) domains in the C-terminus involved in sequence-specific DNA binding and protein-protein interactions. | # |
|
RARA
(details) |
9864 | retinoic acid receptor, alpha | 5914 | P10276 | RARA_HUMAN | zf-C4 PF00105 87-155, Hormone_recep PF00104 227-399 | Rara | 97856 | P11416 | RARA_MOUSE | NR | Nuclear hormone receptors | Histone modification write cofactor, TF | Histone methylation, TF activator, TF repressor | 19377461 | # | histone | H3K4 | H3K4me, H3K4me2 | 19377461 | MLL5 is biochemically identified in a GlcNAcylation-dependent multi-subunit complex associating with nuclear retinoic acid receptor RARalpha (also known as RARA), serving as a mono- and di-methyl transferase to H3K4. | # |
|
REST
(details) |
9966 | RE1-silencing transcription factor | 5978 | Q13127 | REST_HUMAN | zf-C2H2 PF00096 304-326 | Rest | 104897 | Q8VIG1 | REST_MOUSE | # | # | Histone modification erase cofactor, TF | Histone acetylation, TF activator, TF repressor | 12399542 | # | DNA | DNA motif | # | 12399542 | REST/NRSF can mediate repression, in part, through the association of its NH2-terminal repression domain with the mSin3/histone deacethylase 1,2 (HDAC1,2) complex. | # |
|
RUVBL1
(details) |
10474 | RuvB-like AAA ATPase 1 | 8607 | Q9Y265 | RUVB1_HUMAN | TIP49 PF06068 14-368, TIP49_C PF17856 374-439 | Ruvbl1 | 1928760 | P60122 | RUVB1_MOUSE | INO80, AATP | INO80 complex subunits, ATPases / AAA-type | Chromatin remodeling, Histone modification write | Histone phosphorylation | 14695187 | Ino80, SWR, NuA4, NuA4-related complex, CHD8, MLL2/3, MLL4/WBP7, SRCAP | chromatin | # | # | 14695187 | The ability of TIP49=RUVBL1 to inhibit ITF-2 gene expression has been linked to decreased acetylation of histones in the vicinity of the TCF-binding sites in the ITF-2 promoter region. It has been suggested that TIP49 is an important cofactor in beta-catenin/TCF gene regulation in normal and neoplastic cells, likely functioning in chromatin remodeling. | # |
|
SFMBT2
(details) |
20256 | Scm-like with four mbt domains 2 | 57713 | Q5VUG0 | SMBT2_HUMAN | MBT PF02820 78-146 191-258 301-375 411-478, SLED PF12140 529-642, SAM_1 PF00536 823-885 | Sfmbt2 | 2447794 | Q5DTW2 | SMBT2_MOUSE | SAMD | Sterile alpha motif (SAM) domain containing | Histone modification read, Polycomb group (PcG) protein, TF | TF repressor | 23385818 | # | histone, DNA | H3K9me2, H3K9me3, H3K27me3, H4K20me2, H4K20me3 | H3, H4 | 23385818 | SFMBT2 binds preferentially to methylated histone H3 and H4 that are associated with transcriptional repression. Occupancy of SFMBT2 coincide with enrichment of diand tri-methylated H3K9 and H4K20 as well as tri-methylated H3K27 at the HOXB13 gene promoter. | # |
|
SFPQ
(details) |
10774 | splicing factor proline/glutamine-rich | 6421 | P23246 | SFPQ_HUMAN | RRM_1 PF00076 299-363 374-432, NOPS PF08075 444-496 | Sfpq | 1918764 | Q8VIJ6 | SFPQ_MOUSE | RBM | RNA binding motif (RRM) containing | Chromatin remodeling cofactor, RNA modification, TF | TF repressor | 22783022, 10858305, 8449401 | # | DNA, RNA | # | # | 22783022, 10858305, 8449401 | Four components of the Sin3a transcriptional repressor complex: SAP130, SUDS3, SFPQ, and TGIF2. Since the RNA splicing factors do not have an endogenous DNA relaxation activity, topoisomerase I (Chromatin remodeller) gets stimulated by the interaction with the PSF= SFPQ/p54nrb heterodimer. PSF=SFPQ is an essential pre-mRNA splicing factor required early in spliceosome formation. | # |
|
SIN3A
(details) |
19353 | SIN3 transcription regulator family member A | 25942 | Q96ST3 | SIN3A_HUMAN | PAH PF02671 142-186 323-380 478-522, Sin3_corepress PF08295 551-647, Sin3a_C PF16879 885-1192 | Sin3a | 107157 | Q60520 | SIN3A_MOUSE | # | # | Histone modification erase cofactor, TF | Histone acetylation, TF activator, TF repressor | 12670868 | SWI/SNF_Brg1(I), SWI/SNF_Brm, mSin3A, mSin3A-like complex | histone, DNA | DNA motif | # | 12670868 | Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1. | # |
|
SIN3B
(details) |
19354 | SIN3 transcription regulator family member B | 23309 | O75182 | SIN3B_HUMAN | PAH PF02671 60-104 182-235 322-366, Sin3_corepress PF08295 394-447 435-521, Sin3a_C PF16879 775-1081 | Sin3b | 107158 | Q62141 | SIN3B_MOUSE | # | # | Histone modification erase cofactor, TF | Histone acetylation, TF repressor | 12670868 | mSin3A | histone, DNA | DNA motif | # | 12670868 | Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1. | # |
|
SMARCA2
(details) |
11098 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 | 6595 | P51531 | SMCA2_HUMAN | QLQ PF08880 174-208, HSA PF07529 438-508, BRK PF07533 591-633, SNF2-rel_dom PF00176 727-1021, Helicase_C PF00271 1051-1164, SnAC PF14619 1259-1326, Bromodomain PF00439 1421-1489 | Smarca2 | 99603 | Q6DIC0 | SMCA2_MOUSE | # | # | Histone modification read, TF | TF activator | 22464331 | BAF, nBAF, npBAF, WINAC, bBAF, SWI/SNF BRM-BRG1 | histone, DNA | H3, DNA motif | # | 22464331 | Fig. 5 in the reference. | # |
|
SMARCA4
(details) |
11100 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 | 6597 | P51532 | SMCA4_HUMAN | QLQ PF08880 172-205, HSA PF07529 461-532, BRK PF07533 612-653, SNF2-rel_dom PF00176 754-1051, Helicase_C PF00271 1081-1194, SnAC PF14619 1321-1388, Bromodomain PF00439 1477-1547 | Smarca4 | 88192 | Q3TKT4 | SMCA4_MOUSE | # | # | Histone modification read, TF | TF activator | 17582821 | BAF, nBAF, npBAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, SWI/SNF-like_EPAFa, WINAC, SWI/SNF-like EPAFB, bBAF, SWI/SNF BRM-BRG1, CREST-BRG1 | histone | H3, H4 | # | 17582821 | The BRG1 =SMARCA4 bromodomain exhibits binding, albeit weak, to acetylated peptides that are derived from histones H3 and H4. | # |
|
SP1
(details) |
11205 | Sp1 transcription factor | # | P08047 | SP1_HUMAN | zf-C2H2 PF00096 656-680 686-708 | Sp1 | 98372 | O89090 | SP1_MOUSE | SP, ZNF | Specificity protein transcription factors, Zinc fingers, C2H2-type | Chromatin remodeling, TF | TF activator, TF repressor | 17827154, 18850004 | CREST-BRG1 | DNA | DNA motif | # | 17049555 | # | # |
|
SP140
(details) |
17133 | SP140 nuclear body protein | 11262 | Q13342 | SP140_HUMAN | HSR PF03172 38-135, SAND PF01342 583-661, PHD PF00628 693-733, Bromodomain PF00439 779-833 | Sp140 | 3702467 | # | # | PHF | Zinc fingers, PHD-type | Histone modification read, TF | # | 22464331 | # | histone | H3 | # | 22464331 | Fig. 5 in the reference. | # |
|
SPEN
(details) |
17575 | spen family transcriptional repressor | 23013 | Q96T58 | MINT_HUMAN | RRM_1 PF00076 8-67 337-407 439-508 519-583, MINT_MID PF20809 2012-3467, MINT_RID PF20810 2366-2584 3009-3469, MINT_RAM7 PF20808 2654-2749, SPOC PF07744 3506-3662 | Spen | 1891706 | Q62504 | MINT_MOUSE | RBM | RNA binding motif (RRM) containing | Histone modification erase cofactor, TF | Histone acetylation, TF activator, TF repressor | 11331609 | # | histone | # | # | 11331609 | SHARP =SPEN recruits histone deacetylase activity. SHARP is a potent transcriptional repressor whose repression domain (RD) interacts directly with SMRT and at least five members of the NuRD complex including HDAC1 and HDAC2. | # |
|
SUPT3H
(details) |
11466 | suppressor of Ty 3 homolog (S. cerevisiae) | 8464 | O75486 | SUPT3_HUMAN | TFIID-18kDa PF02269 26-115 | # | # | # | # | # | # | Histone modification write cofactor | Histone acetylation | 11564863 | PCAF, SAGA, STAGA | histone | # | # | 11564863 | GCN5 is a histone acetyltransferase (HAT) originally identified in Saccharomyces cerevisiae and required for transcription of specific genes within chromatin as part of the SAGA (SPT-ADA-GCN5 acetylase) coactivator complex. Mammalian cells have two distinct GCN5 homologs (PCAF and GCN5L) that have been found in three different SAGA-like complexes (PCAF complex, TFTC [TATA-binding-protein-free TAFII-containing complex], and STAGA [SPT3-TAFII31-GCN5L acetylase]). | # |
|
SUPT7L
(details) |
30632 | suppressor of Ty 7 (S. cerevisiae)-like | 9913 | O94864 | ST65G_HUMAN | Bromo_TP PF07524 151-228 | Supt7l | 1919445 | Q9CZV5 | ST65G_MOUSE | # | # | Histone chaperone | # | 11564863 | TFTC-HAT, STAGA | histone | # | # | 11564863 | STAGA contains homologs of most yeast SAGA components, including two novel human proteins with histone-like folds and sequence relationships to yeast SPT7 and ADA1. STAGA preferentially acetylates histone H3 within nucleosomes. | # |
|
SUZ12
(details) |
17101 | SUZ12 polycomb repressive complex 2 subunit | 23512 | Q15022 | SUZ12_HUMAN | VEFS-Box PF09733 548-680 | Suz12 | 1261758 | Q80U70 | SUZ12_MOUSE | ZNF | Zinc fingers, C2H2-type | Histone modification write cofactor, Histone modification write cofactor, Polycomb group (PcG) protein, TF | Histone methylation, Histone ubiquitination, TF repressor | 15385962 | PRC2 | DNA | DNA motif | # | 15385962 | SUZ12 is a recently identified Polycomb group (PcG) protein, which together with EZH2 and EED forms different Polycomb repressive complexes (PRC2/3). | # |
|
TADA2A
(details) |
11531 | transcriptional adaptor 2A | 6871 | O75478 | TAD2A_HUMAN | Myb_DNA-binding PF00249 74-118, domain PF22941 165-240, SWIRM PF04433 375-440 | Tada2a | 2144471 | Q8CHV6 | TAD2A_MOUSE | # | # | Histone modification read, TF | TF activator | 19103755 | PCAF, ATAC | histone | H3 | # | 19103755 | The SANT domain of c-Myb has been shown to bind histone H3 tails and position them for acetylation. The SANT domains in ADA2a=TADA2A and ZZZ3/ATAC1 might enable the complex to associate with nucleosome tails in order to potentiate the catalytic activities of GCN5 and ATAC2, similar to what has been shown for the SANT domains in yeast Ada2 and Swi3. | # |
|
TADA2B
(details) |
30781 | transcriptional adaptor 2B | 93624 | Q86TJ2 | TAD2B_HUMAN | Myb_DNA-binding PF00249 68-112, domain PF22941 164-237 | Tada2b | 3035274 | # | # | # | # | Histone modification write cofactor | Histone acetylation | 17694077 | TFTC-HAT | histone | # | # | 17694077 | ADA2b =TADA2B is present in human STAGA/TFTC-type complexes. | # |
|
TADA3
(details) |
19422 | transcriptional adaptor 3 | 10474 | O75528 | TADA3_HUMAN | Ada3 PF10198 311-418 | Tada3 | 1915724 | Q8R0L9 | TADA3_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 11773077 | PCAF, TFTC-HAT, ATAC, STAGA | histone | # | # | 11773077 | Ada2 potentiates the Gcn5 catalytic activity and Ada3 =TADA3 facilitates nucleosomal acetylation and an expanded lysine specificity. | # |
|
TAF10
(details) |
11543 | TAF10 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 30kDa | 6881 | Q12962 | TAF10_HUMAN | TFIID_30kDa PF03540 128-177 | Taf10 | 1346320 | Q8K0H5 | TAF10_MOUSE | # | # | Histone chaperone, Histone modification write | Histone acetylation | 15099517 | PCAF, TFTC-HAT, SAGA, STAGA | histone | H3, H4 | # | 15099517 | SET9 can monomethylate the TBP-associated factor TAF10 at a single lysine residue located at the loop 2 region within the putative histone-fold domain of the protein. | # |
|
TAF12
(details) |
11545 | TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 20kDa | 6883 | Q16514 | TAF12_HUMAN | TFIID_20kDa PF03847 59-126 | Taf12 | 1913714 | Q8VE65 | TAF12_MOUSE | # | # | Histone chaperone, Histone modification write | Histone acetylation | 10594036 | PCAF, STAGA | histone | # | # | 10594036 | Heterodimerization requires the alpha2 and alpha3 helices of the hTAF(II)20 histone fold and is abolished by mutations in the hydrophobic face of the hTAF(II)20 alpha2 helix. Interaction with hTAF(II)20 requires a domain of hTAF(II)135 which shows sequence homology to H2A. | # |
|
TAF2
(details) |
11536 | TAF2 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 150kDa | 6873 | Q6P1X5 | TAF2_HUMAN | Taf2 | 2443028 | Q8C176 | TAF2_MOUSE | # | # | TF | # | # | TFTC-HAT | DNA | DNA motif | # | # | Added because it is a complex partner | # | |
|
TAF4
(details) |
11537 | TAF4 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 135kDa | 6874 | O00268 | TAF4_HUMAN | TAFH PF07531 592-680, TAF4 PF05236 833-1082 | # | # | # | # | # | # | Histone chaperone | # | 10594036 | TFTC-HAT, CHD8, MLL2/3, MLL4/WBP7 | histone | # | # | 10594036 | The histone fold region of hTAFII135 is required for coactivator activity in mammalian cells. | # |
|
TAF5
(details) |
11539 | TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 100kDa | 6877 | Q15542 | TAF5_HUMAN | TFIID_NTD2 PF04494 210-340, WD40 PF00400 466-498 535-571 577-612 618-655 660-697 703-739 | Taf5 | 2442144 | Q8C092 | TAF5_MOUSE | WDR | WD repeat domain containing | Histone modification write cofactor | Histone acetylation | 10373431 | TFTC-HAT | histone | # | # | 10373431 | TFTC, similar to other TBP-free TAFII complexes (yeast SAGA, hSTAGA, and hPCAF) contains the acetyltransferase hGCN5 and is able to acetylate histones in both a free and a nucleosomal context. A monoclonal antibody raised against hTAFII100 recognized hTAFII100=TAF5 not only in TFTC, but detected also a weak band in the PCAF complex. | # |
|
TAF5L
(details) |
17304 | TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, 65kDa | 27097 | O75529 | TAF5L_HUMAN | TFIID_NTD2 PF04494 66-196, WD40 PF00400 269-296 334-370 379-412 418-454 459-496 501-538 | Taf5l | 1919039 | Q91WQ5 | TAF5L_MOUSE | WDR | WD repeat domain containing | Histone modification write cofactor | Histone acetylation | 10373431 | PCAF, TFTC-HAT, STAGA | histone | # | # | 10373431 | The PCAF complex contains hPAF65β=TAF5L, a WD40 repeat-containing factor having similarity to Htafii100(row=423) (5). Antibodies raised against hPAF65β revealed a band around 65 kDa in both the PCAF and the TFTC complexes. | # |
|
TAF6
(details) |
11540 | TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 80kDa | 6878 | P49848 | TAF6_HUMAN | TAF PF02969 12-76, TAF6_C PF07571 214-399 | Taf6 | 109129 | Q62311 | TAF6_MOUSE | # | # | Histone chaperone | # | 9611234 | TFTC-HAT, CHD8, MLL2/3, MLL4/WBP7 | DNA | # | # | 9611234 | The N-CoR/Sin3/HDAc complexes have a key role in the regulation of cellular proliferation and differentiation. N-CoR interacts directly with each of the basal factors, TFIIB and TAFII70 (=TAF6). | # |
|
TAF6L
(details) |
17305 | TAF6-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, 65kDa | 10629 | Q9Y6J9 | TAF6L_HUMAN | TAF PF02969 10-73, TAF6_C PF07571 155-327 | Taf6l | 2444957 | Q8R2K4 | TAF6L_MOUSE | # | # | Histone chaperone | # | 12601814 | PCAF, TFTC-HAT, STAGA | histone | # | # | 12601814 | Human PAF65-alpha shows a strong sequence homology to TAFII80 and also contains a putative HFD. Thus, PAF65-alpha may also interact with TAFII32 in the TFTC complex. | # |
|
TAF7
(details) |
11541 | TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 55kDa | 6879 | Q15545 | TAF7_HUMAN | TAFII55_N PF04658 13-176 | Taf7 | 1346348 | Q9R1C0 | TAF7_MOUSE | # | # | Histone modification write cofactor, Histone modification write cofactor | Histone methylation, Histone acetylation | 22711989 | CHD8, MLL2/3, MLL4/WBP7 | histone | # | # | 22711989 | The largest transcription factor IID (TFIID) subunit, TBP-associated factor 1 (TAF1), possesses protein kinase and histone acetyltransferase (HAT) activities. | # |
|
TAF9
(details) |
11542 | TAF9 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 32kDa | 6880 | Q16594 | TAF9_HUMAN | TFIID-31kDa PF02291 10-130 | Taf9 | 1888697 | Q8VI33 | TAF9_MOUSE | # | # | Histone chaperone | # | 9674425 | PCAF, STAGA, CHD8, MLL2/3, MLL4/WBP7 | DNA | # | # | 9674425 | Histone-like TAFs, including TAFII31 =TAF9, are found within the PCAF histone acetylase complex. | # |
|
TAF9B
(details) |
17306 | TAF9B RNA polymerase II, TATA box binding protein (TBP)-associated factor, 31kDa | 51616 | Q9HBM6 | TAF9B_HUMAN | TFIID-31kDa PF02291 10-130 | Taf9b | 3039562 | Q6NZA9 | TAF9B_MOUSE | # | # | Histone chaperone | # | 15899866 | TFTC-HAT | histone | # | # | 15899866 | TAF9b (formerly TAF9L) is a bona fide TAF that has unique and overlapping roles with TAF9. | # |
|
TFDP1
(details) |
11749 | transcription factor Dp-1 | 7027 | Q14186 | TFDP1_HUMAN | E2F_TDP PF02319 113-193, DP PF08781 200-338 | Tfdp1 | 101934 | Q08639 | TFDP1_MOUSE | # | # | Histone modification | # | 24217316, 22325352 | RING2-L3MBTL2 | histone | # | # | 24217316, 22325352 | Part of a RING2 complex. | # |
|
TFPT
(details) |
13630 | TCF3 (E2A) fusion partner (in childhood Leukemia) | 29844 | P0C1Z6 | TFPT_HUMAN | Tfpt | 1916964 | Q3U1J1 | TFPT_MOUSE | INO80 | INO80 complex subunits | Chromatin remodeling cofactor, DNA modification | DNA hydroxymethylation | 16230350 | Ino80 | chromatin | # | # | 16230350 | Subunit Composition of the hINO80 Complex: These proteins included the “Pim-1 kinase-associated protein-associated protein 1” (PAPA-1, GI 13775202), Amida (also known as TCF3 =TFPT). | # | |
|
TLE4
(details) |
11840 | transducin-like enhancer of split 4 | 7091 | Q04727 | TLE4_HUMAN | TLE_N PF03920 24-138, WD40 PF00400 480-514 534-561 580-605 610-647 695-728 742-769 | Tle4 | 104633 | Q62441 | TLE4_MOUSE | WDR | WD repeat domain containing | Histone modification erase cofactor, TF | # | 24190972 | # | histone | H3ac, H4ac | # | 24190972 | Tle4 is the transcriptional repressor responsible for the establishment of the epigenetic repressive marks at the Ifng locus that result in silencing of Ifng gene expression. Tle proteins have been shown to oligomerize, to associate with amino-terminal domains of histone-modifying proteins, and to form higher-order structures as parts of repressive complexes. | # |
|
TP53
(details) |
11998 | tumor protein p53 | 7157 | P04637 | P53_HUMAN | P53_TAD PF08563 13-33, TAD2 PF18521 23-55, P53 PF00870 101-288, P53_tetramer PF07710 323-357 | Trp53 | 98834 | P02340 | P53_MOUSE | # | # | Histone modification write cofactor, TF | Histone acetylation, TF activator, TF repressor | 23870121 | # | histone | H3 | # | 23870121 | SET1 complex (SET1C)-mediated H3K4 trimethylation is dependent upon p53- and p300-mediated H3 acetylation. Complementary cell-based assays demonstrate a DNA-damage-induced p53-SET1C interaction, a corresponding enrichment of SET1C and H3K4me3 on a p53 target gene (p21/WAF1), and a corresponding codependency of H3K4 trimethylation and transcription upon p300 and SET1C. | # |
|
TRRAP
(details) |
12347 | transformation/transcription domain-associated protein | 8295 | Q9Y4A5 | TRRAP_HUMAN | Tra1_central PF20175 240-895, Tra1_ring PF20206 1003-2695, FAT PF02259 2851-3201, PI3_PI4_kinase PF00454 3531-3782 | Trrap | 2153272 | Q80YV3 | TRRAP_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 14966270 | SWR, PCAF, TFTC-HAT, NuA4, SAGA, NuA4-related complex, STAGA | histone | # | # | 14966270 | The complex(es) contain(s) other subunits shared with NuA4, including TRRAP, p400/hDomino, Brd8. | # |
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VDR
(details) |
12679 | vitamin D (1,25- dihydroxyvitamin D3) receptor | 7421 | P11473 | VDR_HUMAN | zf-C4 PF00105 23-91, Hormone_recep PF00104 227-403 | Vdr | 103076 | P48281 | VDR_MOUSE | NR | Nuclear hormone receptors | Chromatin remodeling cofactor, TF | # | 16252006 | # | histone | H2BK12ac, H3K14ac, H4K16ac | # | 16252006 | WINAC associates with chromatin through a physical interaction between the WSTF bromodomain and acetylated histones, which appears to be indispensable for VDR/promoter association for ligand-induced transrepression of 1α(OH)ase gene expression. | # |
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WHSC1L1
(details) |
12767 | Wolf-Hirschhorn syndrome candidate 1-like 1 | 54904 | Q9BZ95 | NSD3_HUMAN | PWWP PF00855 269-348 962-1050, domain PF23011 700-746, domain PF22908 749-798, domain PF23004 799-851, AWS PF17907 1104-1142, SET PF00856 1155-1262, C5HCH PF17982 1366-1410 | Whsc1l1 | 2142581 | Q6P2L6 | NSD3_MOUSE | # | # | Chromatin remodeling cofactor, TF | # | 16682010 | # | histone | H3K4, H3K27 | # | 16682010 | WHISTLE =WHSC1L1 di-methylates H3K4 and di-, and tri-methylates H3K27 of histones. | # |
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YEATS4
(details) |
24859 | YEATS domain containing 4 | 8089 | O95619 | YETS4_HUMAN | YEATS PF03366 42-121 | Yeats4 | 1927224 | Q9CR11 | YETS4_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 14966270 | NuA4, NuA4-related complex, SRCAP | histone | # | # | 14966270 | The essential GAS41 =YEATS4 protein is a member of the AF9/ENL-related (YEATS) family, and associated to transcription/chromatin-modifying complexes, including yeast NuA4, NuA3, Sas2, SWI/SNF, TFIID/mediator/TFIIF, and human SWI/SNF complexes. | # |
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YY1
(details) |
12856 | YY1 transcription factor | 7528 | P25490 | TYY1_HUMAN | zf-C2H2 PF00096 298-320 325-347 353-377 383-407 | Yy1 | 99150 | Q00899 | TYY1_MOUSE | INO80, ZNF | INO80 complex subunits, Zinc fingers, C2H2-type | Chromatin remodeling cofactor, TF | TF repressor | 11445535 | Ino80 | DNA | DNA motif | # | 11445535 | YY1 is complex comprising components of the evolutionarily conserved INO80 chromatin-remodeling complex. | # |
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ZBTB33
(details) |
16682 | zinc finger and BTB domain containing 33 | 10009 | Q86T24 | KAISO_HUMAN | BTB PF00651 22-116 | Zbtb33 | 1927290 | Q8BN78 | KAISO_MOUSE | ZBTB, BTBD, ZNF | BTB/POZ domain containing, Zinc fingers, C2H2-type | Histone modification write cofactor, Histone modification erase cofactor, TF | Histone acetylation, Histone methylation, TF repressor | 14527417 | # | DNA | CG, mCG, DNA motif | # | 14527417 | Kaiso, a methyl CpG binding protein belonging to the BTB/POZ family of transcription factors, is a component of the human N-CoR complex. In vitro, the Kaiso/N-CoR complex binds specific CpG-rich sequences in a methylation-dependent manner. In vivo, Kaiso targets the N-CoR complex to the MTA2 gene promoter in a methylation-dependent manner. This repression also requires a functional N-CoR deacetylase complex, which brings about histone hypoacetylation and methylation of H3 lysine 9 to the MTA2 locus. | # |
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ZBTB7A
(details) |
18078 | Zinc finger and BTB domain-containing protein 7A (Factor binding IST protein 1) (FBI-1) (Factor that binds to inducer of short transcripts protein 1) (HIV-1 1st-binding protein 1) (Leukemia/lymphoma-related factor) (POZ and Krueppel erythroid myeloid ontogenic factor) (POK erythroid myeloid ontogenic factor) (Pokemon) (Pokemon 1) (TTF-I-interacting peptide 21) (TIP21) (Zinc finger protein 857A) | 51341 | O95365 | ZBT7A_HUMAN | BTB PF00651 24-129, zf-C2H2 PF00096 410-432 438-460 | Zbtb7A | 1335091 | O88939 | ZBT7A_MOUSE | BTBD | BTB domain containing | RNA modification | Alternative splicing | 24514149 | # | RNA | mRNA | # | 24514149 | Regulates alternative splicing of BCL-X and apoptotic factors | New |
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ZFP57
(details) |
18791 | ZFP57 zinc finger protein | 346171 | Q9NU63 | ZFP57_HUMAN | KRAB PF01352 16-56, zf-C2H2 PF00096 91-113 119-141 147-169 175-197 300-322 328-350 | Zfp57 | 99204 | Q8C6P8 | ZFP57_MOUSE | # | # | TF | TF repressor | # | # | DNA | mC, DNA motif | # | # | Acts by controlling DNA methylation during the earliest multicellular stages of development at multiple imprinting control regions. (UniProt) | # |
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ZGPAT
(details) |
15948 | zinc finger, CCCH-type with G patch domain | 84619 | Q8N5A5 | ZGPAT_HUMAN | zf-CCCH_4 PF18044 177-199, G-patch PF01585 333-376 | Zgpat | 2449939 | Q8VDM1 | ZGPAT_MOUSE | ZC3H, GPATCH | Zinc fingers, CCCH-type domain containing, "G patch domain containing" | TF | TF repressor | 22498752 | # | DNA | DNA motif | # | # | Recruits the chromatin multiprotein complex NuRD to target promoters. | # |
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ZMYM2
(details) |
12989 | zinc finger, MYM-type 2 | 7750 | Q9UBW7 | ZMYM2_HUMAN | zf-FCS PF06467 328-364 371-412 422-457 465-504 534-571 637-674 681-716 725-762 766-803, DUF3504 PF12012 1190-1359 | Zmym2 | 1923257 | Q9CU65 | ZMYM2_MOUSE | ZMYM | Zinc fingers, MYM type | Histone modification erase cofactor, TF | Histone acetylation | 12493763 | BHC, LSD-CoREST | DNA | DNA motif | # | 12493763 | A family of HDAC1,2-associated complexes includes proteins with a putative role in DNA binding such as ZNF261/XFIM (=ZMYM3), ZNF198/FIM (=ZMYM2), and ZNF217. | # |
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ZNF217
(details) |
13009 | zinc finger protein 217 | 7764 | O75362 | ZN217_HUMAN | zf-C2H2 PF00096 128-150 156-178 377-397 472-493 | # | # | # | # | ZNF | Zinc fingers, C2H2-type | Histone modification erase cofactor, TF | Histone acetylation, TF repressor | 12493763 | BHC, LSD-CoREST | DNA | # | # | 12493763 | A family of HDAC1,2-associated complexes includes proteins with a putative role in DNA binding such as ZNF261/XFIM (=ZMYM3), ZNF198/FIM (=ZMYM2), and ZNF217. | # |
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ZNF516
(details) |
28990 | zinc finger protein 516 | 9658 | Q92618 | ZN516_HUMAN | zf-C2H2 PF00096 34-56 62-84 248-270 276-298 1098-1120 | Zfp516 | 2443957 | Q7TSH3 | ZN516_MOUSE | ZNF | Zinc fingers, C2H2-type | Histone modification erase cofactor, TF | Histone acetylation, TF repressor | 23752268 | LSD-CoREST | histone, DNA | # | # | 23752268 | Part of the HDAC interactome, TF annotation from Uniprot. | # |