| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
ACTB
(details) |
132 | actin, beta | 60 | P60709 | ACTB_HUMAN | Actin PF00022 4-375 | Actb | 87904 | P60710 | ACTB_MOUSE | # | # | Chromatin remodeling cofactor | # | 10966108 | BAF, nBAF, npBAF, PBAF, SWI/SNF-like EPAFB, bBAF, SWI/SNF BRM-BRG1, NuA4, NuA4-related complex | chromatin | # | # | 10966108 | β-actin=ACTB and actin-related proteins appear to have weak ATPase activities, which contribute ∼1% of the total activity in the BAF remodeling complex (Zhao et al. 1998). Results of experiments using the actin monomer sequestering product latrunculin B suggest that β-actin and BAF53 are required for stimulation of the ATPase activity of the BAF complex by chromatin | # |
|
ACTL6A
(details) |
24124 | actin-like 6A | 86 | O96019 | ACL6A_HUMAN | Actin PF00022 10-428 | Actl6a | 1861453 | Q9Z2N8 | ACL6A_MOUSE | INO80 | INO80 complex subunits | Chromatin remodeling cofactor | # | 9845365 | BAF, npBAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, SWI/SNF-like_EPAFa, WINAC, SWI/SNF-like EPAFB, SWI/SNF BRM-BRG1, Ino80, NuA4, NuA4-related complex, SRCAP | chromatin | # | # | 9845365 | β-actin and BAF53 =ACTL6A are required for maximal ATPase activity of BRG1 and are also required with BRG1 for association of the complex with chromatin/matrix. | # |
|
ACTL6B
(details) |
160 | actin-like 6B | 51412 | O94805 | ACL6B_HUMAN | Actin PF00022 9-425 | Actl6b | 1933548 | Q99MR0 | ACL6B_MOUSE | # | # | Chromatin remodeling cofactor | # | 11726552 | BAF, nBAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, SWI/SNF BRM-BRG1 | chromatin | # | # | 11726552 | Belongs to the chromatin remodeling brain-specific BAF (bBAF) complex, as such plays a role in remodeling mononucleosomes in an ATP-dependent fashion. | # |
|
APOBEC1
(details) |
604 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 | 339 | P41238 | ABEC1_HUMAN | APOBEC4_like PF18774 27-158 | Apobec1 | 103298 | P51908 | ABEC1_MOUSE | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 22001110 | APOB_mRNA_editosome | DNA, RNA | ssDNA, mRNA, mC | U | 22001110 | Fig. A2 in the reference (APOBEC1 or A1 has no known mammalian DNA substrate but it has DNA deaminase activity sufficient to induce reversion mutations when overexpressed in E. coli. In addition, A1 expressed in neurons may have a protective function against HSV (Herpers simplex virus) that involves ssDNA deamination of the viral genome). | # |
|
APOBEC2
(details) |
605 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 2 | 10930 | Q9Y235 | ABEC2_HUMAN | APOBEC2 PF18772 47-223 | Apobec2 | 1343178 | Q9WV35 | ABEC2_MOUSE | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 21496894, 22001110 | # | DNA, RNA | ssDNA, mRNA, mC | hmU | 22001110, 21496894 | Fig. A2 in the reference | # |
|
APOBEC3A
(details) |
17343 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A | 200315 | P31941 | ABC3A_HUMAN | NAD2 PF18782 13-195 | # | # | # | # | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 22001110 | # | DNA, RNA | ssDNA, mRNA, mC | dhU | 22001110 | Fig. A2 in the reference (Targets are exogenous retroviruses ssDNA like HIV, DNA viruses or transposable elements/ endogenous retroelements e.g. LINEs, SINEs and LTR). | # |
|
APOBEC3B
(details) |
17352 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B | 9582 | Q9UH17 | ABC3B_HUMAN | NAD2 PF18782 8-190 193-379 | Apobec3 | 1933111 | Q99J72 | ABEC3_MOUSE | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 22001110 | # | DNA, RNA | ssDNA, mRNA, mC | dhU | 22001110 | Fig. A2 in the reference (Targets are DNA viruses or transposable elements/ endogenous retroelements e.g. LINEs, SINEs and LTR). | # |
|
APOBEC3C
(details) |
17353 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3C | 27350 | Q9NRW3 | ABC3C_HUMAN | NAD2 PF18782 11-189 | # | # | # | # | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 22001110 | # | DNA, RNA | ssDNA, mRNA, mC | dhU | 22001110 | Fig. A2 in the reference (Targets are transposable elements/ endogenous retroelements e.g. LINEs, SINEs and LTR). | # |
|
APOBEC3D
(details) |
17354 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3D | 140564 | Q96AK3 | ABC3D_HUMAN | NAD2 PF18782 10-202 207-381 | # | # | # | # | APOBEC | Apolipoprotein B mRNA editing enzymes | DNA modification, RNA modification | DNA demethylation, mRNA editing | 21835787 | # | 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 and SINEs). | # |
|
APOBEC3F
(details) |
17356 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3F | 200316 | Q8IUX4 | ABC3F_HUMAN | NAD2 PF18782 4-190 192-372 | # | # | # | # | 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, DNA viruses or transposable elements/ endogenous retroelements e.g. LINEs, SINEs and LTR). | # |
|
APOBEC3G
(details) |
17357 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G | 60489 | Q9HC16 | ABC3G_HUMAN | NAD2 PF18782 8-190 200-381 | # | # | # | # | 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, DNA viruses or transposable elements/ endogenous retroelements e.g. SINEs and LTR). | # |
|
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). | # |
|
ARID1A
(details) |
11110 | AT rich interactive domain 1A (SWI-like) | 8289 | O14497 | ARI1A_HUMAN | ARID PF01388 1018-1104, BAF250_C PF12031 1970-2222 | Arid1a | 1935147 | A2BH40 | ARI1A_MOUSE | ARID | # | Chromatin remodeling cofactor | # | 18448678 | BAF, nBAF, npBAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, WINAC, bBAF, SWI/SNF BRM-BRG1 | DNA | DNA motif | # | 18448678 | BAF250a=ARID1A mediated chromatin remodeling plays a critical role in maintaining a particular chromatin configuration of its target genes that is essential for ES pluripotency and mesoderm formation. | # |
|
ARID1B
(details) |
18040 | AT rich interactive domain 1B (SWI1-like) | 57492 | Q8NFD5 | ARI1B_HUMAN | ARID PF01388 1137-1223, BAF250_C PF12031 2006-2266 | Arid1b | 1926129 | # | # | ARID | # | Histone modification write | Histone ubiquitination | 20086098 | BAF, nBAF, npBAF, PBAF, SWI/SNF-like_EPAFa, SWI/SNF-like EPAFB, SWI/SNF BRM-BRG1 | histone, DNA | H2BK120, DNA motif | # | 20086098 | The characteristic member of human SWI/SNF-A is BAF250/ARID1, of which there are two isoforms, BAF250a/ARID1a and BAF250b/ARID1b. The immunopurified BAF250b E3 ubiquitin ligase was found to target histone H2B at lysine 120 for monoubiquitination in vitro. | # |
|
ARID2
(details) |
18037 | AT rich interactive domain 2 (ARID, RFX-like) | 196528 | Q68CP9 | ARID2_HUMAN | ARID PF01388 17-101, RFX_DNA_binding PF02257 524-602 | Arid2 | 1924294 | # | # | ARID | # | Chromatin remodeling cofactor | # | 15640446 | PBAF | DNA | DNA motif | # | 15640446 | Extends the role of ARID-containing subunits as components of SWI/SNF-related chromatin-remodeling complexes. Analysis of ARID2 in the DNA pull-down assay (Figure 4) indicates that it binds DNA without sequence specificity, like all other known ARID-containing components of SWI/SNF-related complexes. | # |
|
ARID4A
(details) |
9885 | AT rich interactive domain 4A (RBP1-like) | 5926 | P29374 | ARI4A_HUMAN | RBB1NT PF08169 171-268, ARID PF01388 311-397, Tudor-knot PF11717 577-631 | Arid4a | 2444354 | # | # | ARID | # | Histone modification write cofactor | Histone acetylation | 15640446 | mSin3A | DNA | DNA motif | # | 15640446 | ARID4 subfamily DNA-binding activity is represented here by RBP1 (ARID4A). Amino acid identity within the ARID consensus is 75% between RBP1 (ARID4A) and RBP1L1 (ARID4B), the only other member of this class. Both RBP1 and RBP1L1/SAP180 have been found in association with the mSIN3-histone deacetylase complex. | # |
|
ARID4B
(details) |
15550 | AT rich interactive domain 4B (RBP1-like) | 51742 | Q4LE39 | ARI4B_HUMAN | RBB1NT PF08169 169-263, ARID PF01388 308-394, Tudor-knot PF11717 572-626 | Arid4b | 2137512 | A2CG63 | ARI4B_MOUSE | ARID | # | Histone modification write cofactor | Histone acetylation | 15640446 | mSin3A | DNA | DNA motif | # | 15640446 | ARID4 subfamily DNA-binding activity is represented here by RBP1 (ARID4A). Amino acid identity within the ARID consensus is 75% between RBP1 (ARID4A) and RBP1L1 (ARID4B), the only other member of this class. Both RBP1 and RBP1L1/SAP180 have been found in association with the mSIN3-histone deacetylase complex. | # |
|
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. | # |
|
ASH1L
(details) |
19088 | ash1 (absent, small, or homeotic)-like (Drosophila) | 55870 | Q9NR48 | ASH1L_HUMAN | AWS PF17907 2105-2142, SET PF00856 2156-2261, Bromodomain PF00439 2462-2533, PHD_5 PF20826 2586-2628, BAH PF01426 2662-2798 | Ash1l | 2183158 | Q99MY8 | ASH1L_MOUSE | KMT, PHF | Chromatin-modifying enzymes / K-methyltransferases, Zinc fingers, PHD-type | Histone modification write | Histone methylation | 21239497 | # | histone | H3K36 | H3K36me | 21239497 | Human ASH1L specifically methylates histone H3 Lys-36. Implicates that there may be a regulatory mechanism of ASH1L histone methyltransferases. | # |
|
ASH2L
(details) |
744 | ash2 (absent, small, or homeotic)-like (Drosophila) | 9070 | Q9UBL3 | ASH2L_HUMAN | PHD_ash2p_like PF21257 105-159, ASH2L-like_WH PF21198 161-266, SPRY PF00622 421-494 | Ash2l | 1344416 | Q91X20 | ASH2L_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification write cofactor | Histone methylation | 21285357 | COMPASS, Menin-associated_HMT, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7, COMPASS-like MLL3,4 | histone | # | # | 21285357 | The oncoprotein Ash2L is a component of the mixed lineage leukemia (MLL) family members 1–4, Setd1A, and Setd1B mammalian histone H3K4 methyltransferase complexes and is essential to maintain global trimethylation of histone H3K4. | # |
|
ASXL1
(details) |
18318 | additional sex combs like transcriptional regulator 1 | 171023 | Q8IXJ9 | ASXL1_HUMAN | HARE-HTH PF05066 11-82, ASXH PF13919 244-363, PHD_3 PF13922 1502-1539 | Asxl1 | 2684063 | P59598 | ASXL1_MOUSE | # | # | Histone modification erase, Polycomb group (PcG) protein | Histone deubiquitination | 20436459 | PR-DUB | histone | H2AK119 | H2AK119ub1 | 20436459 | Reconstituted recombinant Drosophila and human PR-DUB=ASXL1 complexes remove monoubiquitin from H2A but not from H2B in nucleosomes. | # |
|
ASXL2
(details) |
23805 | additional sex combs like transcriptional regulator 2 | 55252 | Q76L83 | ASXL2_HUMAN | HARE-HTH PF05066 11-84, ASXH PF13919 266-381, PHD_3 PF13922 1376-1433 | Asxl2 | 1922552 | Q8BZ32 | ASXL2_MOUSE | # | # | Histone modification read | # | 21047783 | # | histone | H3K4, H3K9 | # | 21047783 | ASXL2 occupies the aP2 promoter together with histone-lysine N-methyltransferase MLL1 and Lys-9-acetylated and Lys-4-methylated H3 histones. Microarray analysis demonstrated that ASXL1 represses, whereas ASXL2 increases, the expression of adipogenic genes. | # |
|
ASXL3
(details) |
29357 | additional sex combs like transcriptional regulator 3 | 80816 | Q9C0F0 | ASXL3_HUMAN | HARE-HTH PF05066 11-82, ASXH PF13919 241-361, PHD_3 PF13922 2204-2246 | Asxl3 | 2685175 | Q8C4A5 | ASXL3_MOUSE | # | # | Scaffold protein, Polycomb group (PcG) protein | # | 23736028 | # | histone | # | # | 23736028 | ASXL family members are epigenetic scaffolding proteins that assemble epigenetic regulators and transcription factors to specific genomic loci with histone modifications, contain PHD domain. | # |
|
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. | # |
|
AURKC
(details) |
11391 | aurora kinase C | 6795 | Q9UQB9 | AURKC_HUMAN | Pkinase PF00069 43-293 | Aurkc | 1321119 | O88445 | AURKC_MOUSE | # | # | Histone modification write | Histone phosphorylation | 15499654 | # | histone | H3S10, H3S28 | # | 15499654 | Aurora-C=AURKC, like Aurora-B kinase, is a chromosomal passenger protein localizing first to centromeres and then to the midzone of mitotic cells. Aurora-C transcript is expressed at a moderate level albeit about an order of magnitude lower than Aurora-B transcript in diploid human fibroblasts. | # |
|
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, | # |
|
BCORL1
(details) |
25657 | BCL6 corepressor-like 1 | 63035 | Q5H9F3 | BCORL_HUMAN | Ank_2 PF12796 1500-1591, PUFD PF16553 1668-1782 | Bcorl1 | 2443910 | A2AQH4 | BCORL_MOUSE | ANKRD | Ankyrin repeat domain containing | Histone modification erase cofactor | Histone deacetylation | 23523425, 17379597 | BCOR | histone | H3K36me2 | # | 23523425 | Homologous to BCOR; which is a component of a complex (dRAF-like complex) in companion with KDM2B, a H3K36me2 demethylase. | # |
|
BMI1
(details) |
1066 | BMI1 proto-oncogene, polycomb ring finger | 648 | P35226 | BMI1_HUMAN | zf-C3HC4_2 PF13923 18-56, RAWUL PF16207 162-226 | Bmi1 | 88174 | P25916 | BMI1_MOUSE | RNF, PCGF | RING-type (C3HC4) zinc fingers, Polycomb group ring fingers | Polycomb group (PcG) protein | # | 15386022 | PRC1 | # | # | # | 15386022 | The complex, termed hPRC1L (human Polycomb repressive complex 1-like), is composed of several Polycomb-group proteins including Ring1, Ring2, Bmi1 and HPH2. | # |
|
BRMS1L
(details) |
20512 | breast cancer metastasis-suppressor 1-like | 84312 | Q5PSV4 | BRM1L_HUMAN | Sds3 PF08598 62-184 | Brms1l | 1196337 | Q3U1T3 | BRM1L_MOUSE | # | # | Histone modification erase | Histone deacetylation | 15451426 | mSin3A | histone | # | # | 15451426 | p40-associated Sin3A/HDAC1 complex can deacetylate histone peptides in vitro. p40 can also repress transcription when tethered to the Gal-regulated promoter by the Gal-DNA binding domain. | # |
|
C11orf30
(details) |
18071 | chromosome 11 open reading frame 30 | 56946 | Q7Z589 | EMSY_HUMAN | ENT PF03735 16-84 | 2210018M11Rik | 1924203 | Q8BMB0 | EMSY_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 19131338 | # | histone | # | # | # | Part of a complex with histone methyltranferase activity. UniProt: Regulator which is able to repress transcription, possibly via its interaction with a multiprotein chromatin remodeling complex that modifies the chromatin. | # |
|
C17orf49
(details) |
28737 | chromosome 17 open reading frame 49 | 124944 | Q8IXM2 | BAP18_HUMAN | 0610010K14Rik | 1915609 | Q9DCT6 | BAP18_MOUSE | # | # | Histone modification read | # | 20850016 | CHD8, MLL2/3, MLL4/WBP7 | histone | H3K4me3 | # | 20850016 | H3K4me3 readers Sgf29, TRRAP, PHF8, GATAD1, and BAP18=C17orf49, are associated mainly with promoters (Figures S3A and S3B) and coincide with H3K4me3 marking. | # | |
|
CBLL1
(details) |
21225 | E3 ubiquitin-protein ligase Hakai (EC 2.3.2.27) (Casitas B-lineage lymphoma-transforming sequence-like protein 1) (c-Cbl-like protein 1) (RING finger protein 188) (RING-type E3 ubiquitin transferase Hakai) | 79872 | Q75N03 | HAKAI_HUMAN | zf_Hakai PF18408 161-191 | Cbll1 | 2144842 | Q9JIY2 | HAKAI_MOUSE | RNF | Ring finger proteins | RNA modification | RNA methylation | 29507755 | WMM | RNA | A of mRNA | m6A | 29507755 | # | New |
|
CDYL
(details) |
1811 | chromodomain protein, Y-like | 9425 | Q9Y232 | CDYL1_HUMAN | Chromo PF00385 61-112, ECH_1 PF00378 363-594 | Cdyl | 1339956 | Q9WTK2 | CDYL_MOUSE | # | # | Histone modification write | Histone acetylation | 12072557 | # | histone | H4 | # | 12072557 | Human CDY and mouse CDYL proteins exhibit histone acetyltransferase activity in vitro, with a strong preference for histone H4. | # |
|
CDYL2
(details) |
23030 | chromodomain protein, Y-like 2 | 124359 | Q8N8U2 | CDYL2_HUMAN | Chromo PF00385 7-57, ECH_1 PF00378 271-500 | Cdyl2 | 1923046 | Q9D5D8 | CDYL2_MOUSE | # | # | Histone modification read | # | 23455924 | # | histone | H3K9me3 | # | 21774827 | Many mouse chromodomain proteins are reported to bind H3K9me3 in vitro, including CDYL, CDYL2, CBX2, CBX4, CBX7 and M-phase phosphoprotein 8 (MPP8). | # |
|
CELF1
(details) |
2549 | CUGBP Elav-like family member 1 (CELF-1) (50 kDa nuclear polyadenylated RNA-binding protein) (Bruno-like protein 2) (CUG triplet repeat RNA-binding protein 1) (CUG-BP1) (CUG-BP- and ETR-3-like factor 1) (Deadenylation factor CUG-BP) (Embryo deadenylation element-binding protein homolog) (EDEN-BP homolog) (RNA-binding protein BRUNOL-2) | 10658 | Q92879 | CELF1_HUMAN | RRM_1 PF00076 19-85 110-174 403-473 | Celf1 | 1342295 | P28659 | CELF1_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CELF2
(details) |
2550 | CUGBP Elav-like family member 2 (CELF-2) (Bruno-like protein 3) (CUG triplet repeat RNA-binding protein 2) (CUG-BP2) (CUG-BP- and ETR-3-like factor 2) (ELAV-type RNA-binding protein 3) (ETR-3) (Neuroblastoma apoptosis-related RNA-binding protein) (hNAPOR) (RNA-binding protein BRUNOL-3) | 10659 | O95319 | CELF2_HUMAN | RRM_1 PF00076 43-110 134-198 425-495 | Celf2 | 1338822 | Q9Z0H4 | CELF2_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CELF3
(details) |
11967 | CUGBP Elav-like family member 3 (CELF-3) (Bruno-like protein 1) (CAG repeat protein 4) (CUG-BP- and ETR-3-like factor 3) (ELAV-type RNA-binding protein 1) (ETR-1) (Expanded repeat domain protein CAG/CTG 4) (RNA-binding protein BRUNOL-1) (Trinucleotide repeat-containing gene 4 protein) | 11189 | Q5SZQ8 | CELF3_HUMAN | RRM_1 PF00076 9-75 97-161 382-452 | Celf3 | 1926034 | Q8CIN6 | CELF3_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CELF4
(details) |
14015 | CUGBP Elav-like family member 4 (CELF-4) (Bruno-like protein 4) (CUG-BP- and ETR-3-like factor 4) (RNA-binding protein BRUNOL-4) | 56853 | Q9BZC1 | CELF4_HUMAN | RRM_1 PF00076 56-121 154-216 442-473 | Celf4 | 1932407 | Q7TSY6 | CELF4_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CELF5
(details) |
14058 | CUGBP Elav-like family member 5 (CELF-5) (Bruno-like protein 5) (CUG-BP- and ETR-3-like factor 5) (RNA-binding protein BRUNOL-5) | 60680 | Q8N6W0 | CELF5_HUMAN | RRM_1 PF00076 47-112 136-198 402-472 | Celf5 | 2442333 | D3Z4T1 | D3Z4T1_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CELF6
(details) |
14059 | CUGBP Elav-like family member 6 (CELF-6) (Bruno-like protein 6) (CUG-BP- and ETR-3-like factor 6) (RNA-binding protein BRUNOL-6) | 60677 | Q96J87 | CELF6_HUMAN | RRM_1 PF00076 48-113 136-199 398-468 | Celf6 | 1923433 | Q7TN33 | CELF6_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 11158314, 12649496 | # | RNA | mRNA | # | 11158314, 12649496 | Regulates MSE-dependent alternative splicing of cTNT during development in vertebrates. | New |
|
CHD1
(details) |
1915 | chromodomain helicase DNA binding protein 1 | 1105 | O14646 | CHD1_HUMAN | Chromo PF00385 313-351 389-443, SNF2-rel_dom PF00176 482-764, Helicase_C PF00271 789-902, CDH1_2_SANT_HL1 PF18375 1124-1211, CHD1-like_C PF13907 1409-1500 | Chd1 | 88393 | P40201 | CHD1_MOUSE | # | # | Chromatin remodeling | # | 12592387 | # | DNA | # | # | 12592387 | These proteins have a DNA-binding domain as well as a chromodomain motif that can directly effect chromatin structure and gene transcription. There are currently four known members of this gene family in humans (CHD1–CHD4). | # |
|
CHD1L
(details) |
1916 | chromodomain helicase DNA binding protein 1-like | 9557 | Q86WJ1 | CHD1L_HUMAN | SNF2-rel_dom PF00176 49-327, Helicase_C PF00271 348-459 | Chd1l | 1915308 | Q9CXF7 | CHD1L_MOUSE | # | # | Chromatin remodeling | # | 19661379 | # | DNA | # | # | 19661379 | A chromatin-remodeling enzyme, ALC1 (Amplified in Liver Cancer 1, also known as CHD1L), that interacts with poly(ADP-ribose) and catalyzes PARP1-stimulated nucleosome sliding. | # |
|
CHD2
(details) |
1917 | chromodomain helicase DNA binding protein 2 | 1106 | O14647 | CHD2_HUMAN | Chromo PF00385 300-338 378-447, SNF2-rel_dom PF00176 487-767, Helicase_C PF00271 792-905, CDH1_2_SANT_HL1 PF18375 1129-1219, CHD1-like_C PF13907 1465-1553 | Chd2 | 2448567 | E9PZM4 | CHD2_MOUSE | # | # | Chromatin remodeling | # | 12592387 | # | DNA | # | # | 12592387 | These proteins have a DNA-binding domain as well as a chromodomain motif that can directly effect chromatin structure and gene transcription. There are currently four known members of this gene family in humans (CHD1–CHD4). | # |
|
CHD3
(details) |
1918 | chromodomain helicase DNA binding protein 3 | 1107 | Q12873 | CHD3_HUMAN | CHDNT PF08073 155-201, PHD PF00628 382-423 458-500, Chromo PF00385 630-682, SNF2-rel_dom PF00176 738-1034, Helicase_C PF00271 1061-1174, DUF1087 PF06465 1294-1350, CHDII_SANT-like PF06461 1376-1517, CHDCT2 PF08074 1737-1884 | Chd3 | 1344395 | # | # | PHF | Zinc fingers, PHD-type | Chromatin remodeling | # | 12592387 | NuRD | DNA | # | # | 12592387 | These proteins have a DNA-binding domain as well as a chromodomain motif that can directly effect chromatin structure and gene transcription. There are currently four known members of this gene family in humans (CHD1–CHD4). | # |
|
CHD4
(details) |
1919 | chromodomain helicase DNA binding protein 4 | 1108 | Q14839 | CHD4_HUMAN | CHDNT PF08073 165-217, PHD PF00628 373-414 452-493, Chromo PF00385 621-673, SNF2-rel_dom PF00176 728-1024, Helicase_C PF00271 1052-1164, DUF1087 PF06465 1291-1350, CHDII_SANT-like PF06461 1379-1520, CHDCT2 PF08074 1726-1872 | Chd4 | 1344380 | Q6PDQ2 | CHD4_MOUSE | PHF | Zinc fingers, PHD-type | Chromatin remodeling | # | 12592387 | NuRD | DNA | # | # | 12592387 | These proteins have a DNA-binding domain as well as a chromodomain motif that can directly effect chromatin structure and gene transcription. There are currently four known members of this gene family in humans (CHD1–CHD4). | # |
|
CHD5
(details) |
16816 | chromodomain helicase DNA binding protein 5 | 26038 | Q8TDI0 | CHD5_HUMAN | CHDNT PF08073 149-200, PHD PF00628 346-387 418-460, Chromo PF00385 590-643, SNF2-rel_dom PF00176 701-998, Helicase_C PF00271 1025-1138, DUF1087 PF06465 1299-1354, CHDII_SANT-like PF06461 1383-1527, CHDCT2 PF08074 1733-1879 | Chd5 | 3036258 | A2A8L1 | CHD5_MOUSE | PHF | Zinc fingers, PHD-type | Chromatin remodeling | # | 12592387 | # | histone | H3K27me3, H3K4 | # | 12592387, 23948251 | A novel gene encoding a protein with chromatin remodeling, helicase and DNA-binding motifs. This gene (CHD5) is the fifth member of the CHD gene family identified in humans. | # |
|
CHUK
(details) |
1974 | conserved helix-loop-helix ubiquitous kinase | 1147 | O15111 | IKKA_HUMAN | Pkinase PF00069 16-290, IKBKB_SDD PF18397 387-658, IKKbetaNEMObind PF12179 708-744 | Chuk | 99484 | Q60680 | IKKA_MOUSE | # | # | Histone modification write | Histone phosphorylation | 17434128 | # | histone | H3 | # | 17434128 | In the nucleus, IKKα=CHUK is recruited to the promoter region of the NF-κB-regulated genes by interacting with CBP, and contributes to NF-κB-mediated gene expressions through phosphorylation of histone H3. | # |
|
CTCFL
(details) |
16234 | CCCTC-binding factor (zinc finger protein)-like | 140690 | Q8NI51 | CTCFL_HUMAN | zf-C2H2 PF00096 313-336 342-364 398-421 428-451 546-566 | Ctcfl | 3652571 | A2APF3 | CTCFL_MOUSE | ZNF | Zinc fingers, C2H2-type | Chromatin remodeling | # | 18765639 | # | DNA | # | # | 18765639 | BORIS=CTCFL acts as a scaffold upon which BAT3 and SET1A assemble and through which BAT3 and SET1A exert their effects upon chromatin structure and gene expression. In contrast to CTCF, BORIS appears to be a methylation-independent DNA-binding protein (28b) that activates, rather than inhibits, gene expression. | # |
|
DDX21
(details) |
2744 | DEAD (Asp-Glu-Ala-Asp) box helicase 21 | 9188 | Q9NR30 | DDX21_HUMAN | DEAD PF00270 211-383, Helicase_C PF00271 434-532, GUCT PF08152 620-708 | Ddx21 | 1860494 | Q9JIK5 | DDX21_MOUSE | DDX | DEAD-boxes | RNA modification | # | 11237763 | B-WICH | RNA | # | # | 11237763 | Human RNA helicase II/Gu (hRH II/Gu) protein unwinds double-stranded RNA, folds single-stranded RNA, and may play important roles in ribosomal RNA biogenesis, RNA editing, RNA transport, and general transcription. | # |
|
DMAP1
(details) |
18291 | DNA methyltransferase 1 associated protein 1 | 55929 | Q9NPF5 | DMAP1_HUMAN | SANT_DAMP1_like PF16282 124-202, DMAP1 PF05499 242-400 | Dmap1 | 1913483 | Q9JI44 | DMAP1_MOUSE | # | # | Chromatin remodeling | # | 14966270 | NuA4, NuA4-related complex, SRCAP | chromatin | # | # | 14966270 | SANT-domain protein DMAP1 links NuA4 to DNA replication and is also present in distinct proteins | # |
|
DNMT3L
(details) |
2980 | DNA (cytosine-5-)-methyltransferase 3-like | 29947 | Q9UJW3 | DNM3L_HUMAN | ADD_DNMT3 PF17980 37-87, ADDz_Dnmt3b PF21255 96-146 | Dnmt3l | 1859287 | Q9CWR8 | DNM3L_MOUSE | # | # | Histone modification read | # | 17687327 | # | histone | H3K4 | # | 17687327 | DNMT3L specifically interacts with the extreme amino terminus of histone H3, this interaction is strongly inhibited by methylation at lysine 4 of histone H3. | # |
|
DOT1L
(details) |
24948 | DOT1-like histone H3K79 methyltransferase | 84444 | Q8TEK3 | DOT1L_HUMAN | DOT1 PF08123 117-317 | Dot1l | 2143886 | - | - | KMT | Chromatin-modifying enzymes / K-methyltransferases | Histone modification write | Histone methylation | 12123582 | # | histone | H3K79 | # | 12123582 | Human DOT1-like (DOT1L) protein possesses intrinsic H3-K79-specific histone methyltransferase (HMTase) activity in vitro and in vivo. | # |
|
DPY30
(details) |
24590 | dpy-30 homolog (C. elegans) | 84661 | Q9C005 | DPY30_HUMAN | Dpy-30 PF05186 52-92 | Dpy30 | 1913560 | Q99LT0 | DPY30_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 19556245 | COMPASS, Menin-associated_HMT, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7, COMPASS-like MLL3,4 | histone | # | # | 19556245 | The isolated MLL1 SET domain is an H3K4 monomethyltransferase. When the MLL1 SET domain fragment is assembled with a complex containing WDR5, RbBP5, Ash2L, and DPY-30, the rate of lysine methylation is dramatically increased, but only to the dimethyl form of H3K4, suggesting that the MLL1 core complex is predominantly a dimethyltransferase. | # |
|
DTX3L
(details) |
30323 | deltex 3 like, E3 ubiquitin ligase | 151636 | Q8TDB6 | DTX3L_HUMAN | DTX3L_a-b PF21717 134-194, DTX3L_KH-like PF21718 235-357 373-508, zf-C3HC4_2 PF13923 561-599, DTC PF18102 608-739 | Dtx3l | 2656973 | Q3UIR3 | DTX3L_MOUSE | RNF | RING-type (C3HC4) zinc fingers | Histone modification write | Histone ubiquitination | 19818714 | # | histone | H4K91 | # | 19818714 | BBAP=DTX3L selectively monoubiquitylates histone H4 lysine 91 and protects cells exposed to DNA-damaging agents. | # |
|
EEF1AKMT3
(details) |
24936 | EEF1A lysine methyltransferase 3 | 25895 | Q96AZ1 | EFMT3_HUMAN | Methyltransf_16 PF10294 38-195 | Eef1akmt3 | 3645330 | D3YWP0 | EFMT3_MOUSE | METTL | Methyltransferase like | Protein modification | Protein methylation | 28108655 | # | protein | Lys165 of eEF1A | K165m | 28108655 | Modulates mRNA translation | New |
|
EEF1AKNMT
(details) |
24248 | eEF1A lysine and N-terminal methyltransferase | 51603 | Q8N6R0 | EFNMT_HUMAN | domain PF13649 53-157, Spermine_synth PF01564 493-616 | Eef1aknmt | 1918699 | Q91YR5 | EFNMT_MOUSE | METTL | Methyltransferase like | Protein modification | Protein methylation | 30143613 | # | protein | Lys55 of eEF1A | K55m | 30143613 | Modulates mRNA translation | New |
|
EHMT1
(details) |
24650 | euchromatic histone-lysine N-methyltransferase 1 | 79813 | Q9H9B1 | EHMT1_HUMAN | EHMT1-2_CRR PF21533 539-633, Ank_4 PF13637 772-836, Ank_2 PF12796 838-904 907-990, Pre-SET PF05033 1015-1118, SET PF00856 1137-1243 | Ehmt1 | 1924933 | Q5DW34 | EHMT1_MOUSE | KMT, ANKRD | Chromatin-modifying enzymes / K-methyltransferases, Ankyrin repeat domain containing | Histone modification write | Histone methylation | 18264113 | # | histone | H3K9 | H3K9me1, H3K9me2 | 18264113 | G9a and G9a-like protein (GLP)=EHMT1 are euchromatin-associated methyltransferases that repress transcription by mono- and dimethylating histone H3 at Lys9 (H3K9). | # |
|
EHMT2
(details) |
14129 | euchromatic histone-lysine N-methyltransferase 2 | 10919 | Q96KQ7 | EHMT2_HUMAN | EHMT1-2_CRR PF21533 447-540, Ank_2 PF12796 655-746 750-816, Ank PF00023 850-882, Pre-SET PF05033 927-1030, SET PF00856 1049-1155 | Ehmt2 | 2148922 | Q9Z148 | EHMT2_MOUSE | KMT, ANKRD | Chromatin-modifying enzymes / K-methyltransferases, Ankyrin repeat domain containing | Histone modification write | Histone methylation | 18264113 | # | histone | H3K9 | H3K9me1, H3K9me2 | 18264113 | G9a=EHMT2 and G9a-like protein (GLP) are euchromatin-associated methyltransferases that repress transcription by mono- and dimethylating histone H3 at Lys9 (H3K9). | # |
|
EIF4A3
(details) |
18683 | Eukaryotic initiation factor 4A-III (eIF-4A-III) (eIF4A-III) (EC 3.6.4.13) (ATP-dependent RNA helicase DDX48) (ATP-dependent RNA helicase eIF4A-3) (DEAD box protein 48) (Eukaryotic initiation factor 4A-like NUK-34) (Eukaryotic translation initiation factor 4A isoform 3) (Nuclear matrix protein 265) (NMP 265) (hNMP 265) [Cleaved into: Eukaryotic initiation factor 4A-III, N-terminally processed] | 9775 | P38919 | IF4A3_HUMAN | DEAD PF00270 63-225, Helicase_C PF00271 264-372 | EIf4A3 | 1923731 | Q91VC3 | IF4A3_MOUSE | DDX | DEAD-box helicases | RNA modification | Alternative splicing | 22203037 | # | RNA | mRNA | # | 22203037 | Production of the proapoptotic Bcl-x(S) splice variant. | New |
|
ELP5
(details) |
30617 | elongator acetyltransferase complex subunit 5 | 23587 | Q8TE02 | ELP5_HUMAN | Elong_Iki1 PF10483 11-181 222-281 | Elp5 | 1859017 | Q99L85 | ELP5_MOUSE | ELP | Elongator acetyltransferase complex subunits | Histone modification write cofactor | Histone acetylation | 11904415 | Pol2 elongator | histone | H3K14, H4K8 | # | 11904415 | The elongating, hyperphosphorylated form of RNA polymerase II is associated with the Elongator complex, which has the histone acetyltransferase (HAT) Elp3 as a subunit. The three smallest Elongator subunits--Elp4, Elp5, and Elp6--are required for HAT activity, and Elongator binds to both naked and nucleosomal DNA. Elongator may play a role in chromatin remodeling and is involved in acetylation of histones H3 and probably H4. | # |
|
EPC1
(details) |
19876 | enhancer of polycomb homolog 1 (Drosophila) | 80314 | Q9H2F5 | EPC1_HUMAN | EPL1 PF10513 6-148, E_Pc_C PF06752 581-836 | Epc1 | 1278322 | Q8C9X6 | EPC1_MOUSE | # | # | Polycomb group (PcG) protein | # | 14966270 | NuA4, Piccolo_NuA4, NuA4-related complex | histone | # | # | 14966270 | The Enhancer of Polycomb homology domain of human EPC1, like Epl1 in yeast (7), is a conserved functional key for histone acetylation since it bridges the MYST HAT with the ING protein to enable potent nucleosome histone acetyltransferase activity. | # |
|
ERBB4
(details) |
3432 | v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 | 2066 | Q15303 | ERBB4_HUMAN | Recep_L_domain PF01030 55-166 358-477, Furin-like PF00757 184-335, GF_recep_IV PF14843 502-633, TM_ErbB1 PF21314 653-687, PK_Tyr_Ser-Thr PF07714 718-974 | Erbb4 | 104771 | Q61527 | ERBB4_MOUSE | # | # | Histone modification cofactor | # | 23230144 | # | histone | H3K9me3 | # | 23230144 | ErbB4 intracellular domain (4ICD) that translocates into the nucleus to control gene expression through inhibiting an increase of H3K9me3. | # |
|
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. | # |
|
FAM175B
(details) |
28975 | family with sequence similarity 175, member B | 23172 | Q15018 | F175B_HUMAN | MPN_2A_DUB_like PF21125 3-167 | Fam175b | 1926116 | Q3TCJ1 | F175B_MOUSE | # | # | Histone modification erase cofactor | Histone ubiquitination | 20656690 | BRISC | histone | H2AK63 | H2AK63ub | 20656690 | # | # |
|
FBRSL1
(details) |
29308 | fibrosin-like 1 | 57666 | Q9HCM7 | FBSL_HUMAN | Auts2 PF15336 587-788 | Fbrsl1 | 1920907 | # | # | # | # | Histone modification | # | 24217316, 22325352 | RING2-FBRS | histone | # | # | 24217316, 22325352 | Part of a RING2 complex. | # |
|
HCFC1
(details) |
4839 | host cell factor C1 | 3054 | P51610 | HCFC1_HUMAN | Kelch_1 PF01344 32-69, Kelch_5 PF13854 78-114 319-361, Kelch_3 PF13415 216-263 | Hcfc1 | 105942 | Q61191 | HCFC1_MOUSE | # | # | Chromatin remodeling | # | 12670868 | NSL, COMPASS, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7 | chromatin | # | # | 12670868 | A series of molecular activities are associated with the N-terminal subunit of HCF-1 in HSV uninfected cells. Two of these activities are associated with opposing roles in the regulation of transcription through the modulation of chromatin structure: Sin3 HDAC and a novel human Set1/Ash2 HMT. | # |
|
HDAC1
(details) |
4852 | histone deacetylase 1 | 3065 | Q13547 | HDAC1_HUMAN | Hist_deacetyl PF00850 28-318 | Hdac1 | 108086 | O09106 | HDAC1_MOUSE | # | # | Histone modification erase | Histone acetylation | 10220385 | SWI/SNF_Brm, NuRD, BHC, MeCP1, mSin3A, core HDAC, mSin3A-like complex, RING2-L3MBTL2, CREST-BRG1, LSD-CoREST | histone | H3, H4 | # | 10220385 | HDAC1, HDAC4, HDAC5, and HDAC6 deacetylate all four core histones equally well, though deacetylation by HDAC4 and HDAC5 is incomplete. | # |
|
HDAC2
(details) |
4853 | histone deacetylase 2 | 3066 | Q92769 | HDAC2_HUMAN | Hist_deacetyl PF00850 29-319 | Hdac2 | 1097691 | P70288 | HDAC2_MOUSE | # | # | Histone modification erase | Histone acetylation | 9346952 | SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, NuRD, BHC, MeCP1, mSin3A, core HDAC, mSin3A-like complex, RING2-L3MBTL2, LSD-CoREST | histone | H2AKac, H2BKac, H3Kac, H4Kac | H2AK, H2BK, H3K, H4K | 9346952 | HDAC1, HDAC2, and HDAC3 constitute a human HDAC family. All three proteins possess histone deacetylase activity, and repress transcription when bound to a promoter. | # |
|
HDGFL2
(details) |
14680 | HDGF like 2 | 84717 | Q7Z4V5 | HDGR2_HUMAN | PWWP PF00855 7-86, LEDGF PF11467 472-568 | Hdgfrp2 | 1194492 | Q3UMU9 | HDGR2_MOUSE | # | # | Histone modification read | # | 217205545 | # | histone | H3K79me3, H4K20me3, H3K36me3 | # | 217205545 | The crystal structures of the PWWP domains from seven different human proteins and three PWWP domain complex structures with histone peptides, i.e., BRPF1-H3K36me3, HDGF2-H3K79me3 and HDGF2-H4K20me3 shows that the PWWP domain can not only bind DNA but also histones. | # |
|
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. | # |
|
IKBKAP
(details) |
5959 | inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein | 8518 | O95163 | ELP1_HUMAN | IKI3 PF04762 2-955 | Ikbkap | 1914544 | Q7TT37 | ELP1_MOUSE | ELP | Elongator acetyltransferase complex subunits | Scaffold protein | # | 11818576, 11714725 | Pol2 elongator | # | RNA | # | 11818576, 11714725 | The human Elongator facilitates transcription by RNA polymerase II in a chromatin- and acetyl-CoA-dependent manner. Several human homologues of the yeast Elongator subunits have been identified as subunits of the human Elongator complex, including StIP1 (STAT-interacting protein 1) and IKAP (IKK complex-associated protein) =IKBKAP. | # |
|
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) | # |
|
ING2
(details) |
6063 | inhibitor of growth family, member 2 | 3622 | Q9H160 | ING2_HUMAN | ING PF12998 27-122 | Ing2 | 1916510 | Q9ESK4 | ING2_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification read | # | 16728974 | mSin3A-like complex | histone | H3K4me3 | # | 16728974 | ING2, a native subunit of a repressive mSin3a-HDAC1 histone deacetylase complex, binds with high affinity to the trimethylated species. In response to DNA damage, recognition of H3K4me3 by the ING2 PHD domain stabilizes the mSin3a-HDAC1 complex at the promoters of proliferation genes. | # |
|
JADE1
(details) |
30027 | jade family PHD finger 1 | 79960 | Q6IE81 | JADE1_HUMAN | EPL1 PF10513 17-181, PHD_2 PF13831 218-251, zf-HC5HC2H_2 PF13832 256-369 | Jade1 | 1925835 | Q6ZPI0 | JADE1_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification write | Histone acetylation | 16387653 | HBO1 | histone | H3, H4 | H3ac, H4ac | 16387653 | HBO1-JADE(1,2,3=PHF15,PHF16,PHF17)-ING-hEAF6 tetramer complexes are likely responsible for the majority of histone H4 acetylation higher eukaryotes. | # |
|
JADE2
(details) |
22984 | jade family PHD finger 2 | 23338 | Q9NQC1 | JADE2_HUMAN | EPL1 PF10513 16-177, PHD_2 PF13831 214-247, zf-HC5HC2H_2 PF13832 253-364 | Jade2 | 1924151 | Q6ZQF7 | JADE2_MOUSE | PHF | Zinc fingers, PHD-type | Histone modification write | Histone acetylation | 16387653 | HBO1 | histone | H3, H4 | H3ac, H4ac | 16387653 | HBO1-JADE(1,2,3=PHF15,PHF16,PHF17)-ING-hEAF6 tetramer complexes are likely responsible for the majority of histone H4 acetylation higher eukaryotes. | # |
|
KAT8
(details) |
17933 | K(lysine) acetyltransferase 8 | 84148 | Q9H7Z6 | KAT8_HUMAN | Tudor-knot PF11717 54-110, zf-MYST PF17772 176-230, MOZ_SAS PF01853 235-412 | Kat8 | 1915023 | Q9D1P2 | KAT8_MOUSE | KAT, ZC2HC | Chromatin-modifying enzymes / K-acetyltransferases, Zinc fingers, C2HC-type containing | Histone modification write | Histone acetylation | 10786633 | NSL, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7 | histone | H2A, H3, H4 | H2Aac, H3ac, H4ac | 10786633 | A recombinant C-terminal portion of hMOF=KAT8 has histone acetyltransferase activity directed toward histones H3, H2A and H4, a specificity characteristic of other MYST family histone acetyltransferases. | # |
|
KDM2A
(details) |
13606 | lysine (K)-specific demethylase 2A | 22992 | Q9Y2K7 | KDM2A_HUMAN | JHD PF17811 304-343, zf-CXXC PF02008 565-609, PHD_4 PF16866 615-676, F-box-like PF12937 896-935 | Kdm2a | 1354736 | P59997 | KDM2A_MOUSE | FBXL, KDM | F-boxes / Leucine-rich repeats, Chromatin-modifying enzymes / K-demethylases | Histone modification erase | Histone methylation | 20417597 | # | histone | H3K36me2 | H3K36 | 20417597 | CpG islands directly recruit the H3K36-specific lysine demethylase enzyme KDM2A. Nucleation of KDM2A at these elements results in removal of H3K36 methylation, creating CpG island chromatin that is uniquely depleted of this modification. | # |
|
KDM2B
(details) |
13610 | lysine (K)-specific demethylase 2B | 84678 | Q8NHM5 | KDM2B_HUMAN | Cupin_8 PF13621 150-331, JHD PF17811 334-375, zf-CXXC PF02008 607-651, PHD_4 PF16866 657-723, F-box-like PF12937 1068-1107 | Kdm2b | 1354737 | Q6P1G2 | KDM2B_MOUSE | FBXL, KDM | F-boxes / Leucine-rich repeats, Chromatin-modifying enzymes / K-demethylases | Histone modification erase | Histone methylation | 17994099 | BCOR | histone | H3K4me3, H3K36me2 | H3K4, H3K36 | 17994099 | JHDM1B =KDM2B is a histone demethylase that catalyses the demethylation of H3K4me3. | # |
|
KDM6A
(details) |
12637 | lysine (K)-specific demethylase 6A | 7403 | O15550 | KDM6A_HUMAN | TPR_8 PF13181 205-237, JmjC PF02373 1133-1241, KDM6_C-hel PF21322 1248-1303, KDM6_GATAL PF21326 1320-1380 | Kdm6a | 1095419 | O70546 | KDM6A_MOUSE | KDM, TTC | Chromatin-modifying enzymes / K-demethylases, Tetratricopeptide (TTC) repeat domain containing | Histone modification erase | Histone methylation | 17851529 | CHD8, MLL2/3, MLL4/WBP7, COMPASS-like MLL3,4 | histone | H3K27me2. H3K27me3 | H3K27 | 17851529 | The JmjC-domain-containing proteins UTX=KDM6A and JMJD3 catalyse demethylation of H3K27me3/2. | # |
|
KEAP1
(details) |
23177 | kelch-like ECH-associated protein 1 | 9817 | Q14145 | KEAP1_HUMAN | BTB PF00651 67-178, BACK PF07707 184-285, Kelch_1 PF01344 327-359 361-410 412-457 459-504 507-551 553-598 | Keap1 | 1858732 | Q9Z2X8 | KEAP1_MOUSE | KLHL, BTBD | Kelch-like, "BTB/POZ domain containing" | Chromatin remodeling | # | 21920360 | # | chromatin | # | # | # | Interacts with the NURF Nucleosome Remodeling Factor complex. | # |
|
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 |
|
KMT2A
(details) |
7132 | lysine (K)-specific methyltransferase 2A | 4297 | Q03164 | KMT2A_HUMAN | zf-CXXC PF02008 1149-1194, PHD PF00628 1481-1530 1569-1624, zf-HC5HC2H PF13771 1897-1978, FYRN PF05964 2016-2077, FYRC PF05965 3666-3747, SET PF00856 3840-3945 | Kmt2a | 96995 | P55200 | KMT2A_MOUSE | KMT, PHF | Chromatin-modifying enzymes / K-methyltransferases, Zinc fingers, PHD-type | Histone modification write | Histone methylation | 19187761 | MLL-HCF, CHD8, COMPASS-like MLL1,2 | histone | H3K4 | H3K4me | 19187761 | MLL1 SET domain can incorporate methyl groups into unmodified or H3K4me1 substrates, signifying both mono- and dimethylation activity. | # |
|
KMT2B
(details) |
15840 | lysine (K)-specific methyltransferase 2B | 9757 | Q9UMN6 | KMT2B_HUMAN | zf-CXXC PF02008 959-1005, PHD PF00628 1203-1250 1251-1300 1337-1393, zf-HC5HC2H PF13771 1605-1685, FYRN PF05964 1731-1784, FYRC PF05965 2415-2494, SET PF00856 2580-2691 | Kmt2b | 109565 | O08550 | KMT2B_MOUSE | KMT | Chromatin-modifying enzymes / K-methyltransferases | Histone modification write | Histone methylation | 17707229 | Menin-associated_HMT, MLL2/3, COMPASS-like MLL3,4 | histone | H3K4 | H3K4me3 | 17707229 | MLL (=KMT2B)-containing complexes methylate histone H3 at lysine 4 (H3K4) and have been implicated in the regulation of transcription. | # |
|
KMT2C
(details) |
13726 | lysine (K)-specific methyltransferase 2C | 58508 | Q8NEZ4 | KMT2C_HUMAN | zf-HC5HC2H PF13771 248-331, PHD PF00628 343-389 390-436 466-519 958-1008, zf-HC5HC2H_2 PF13832 4401-4506, FYRN PF05964 4546-4604, FYRC PF05965 4608-4692, SET PF00856 4781-4887 | Kmt2c | 2444959 | Q8BRH4 | KMT2C_MOUSE | KMT, PHF | Chromatin-modifying enzymes / K-methyltransferases, Zinc fingers, PHD-type | Histone modification write | Histone methylation | 20937768 | MLL2/3, COMPASS-like MLL3,4 | histone | H3K4 | H3K4me | 20937768 | In humans, multiple Set1-like HMT complexes with H3K4 HMT activities have been identified. Each of these complexes contains the SET domain-containing homologs of yeast Set1, including human Set1 (hSet1), MLL1 (mixed lineage leukemia 1, also known as MLL, HRX, ALL1, or KMT2A), MLL2 (mixed-lineage leukemia 2, also known as HRX2 or KMT2B), MLL3 (mixed-lineage leukemia 3, also known as HALR or KMT2C), and MLL4 (mixed-lineage leukemia 4, also known as ALR or KMT2D), which carry the enzymatic activity for the associated complexes. | # |
|
KMT2D
(details) |
7133 | lysine (K)-specific methyltransferase 2D | 8085 | O14686 | KMT2D_HUMAN | zf-HC5HC2H PF13771 139-218, PHD PF00628 228-274 276-321 1379-1428 1429-1474, zf-HC5HC2H_2 PF13832 5031-5136, FYRN PF05964 5176-5233, FYRC PF05965 5236-5322, SET PF00856 5408-5513 | Kmt2d | 2682319 | Q6PDK2 | KMT2D_MOUSE | KMT, PHF | Chromatin-modifying enzymes / K-methyltransferases, Zinc fingers, PHD-type | Histone modification write | Histone methylation | 20937768 | COMPASS-like MLL1,2, MLL4/WBP7, COMPASS-like MLL3,4 | histone | H3K4 | H3K4me | 20937768 | In humans, multiple Set1-like HMT complexes with H3K4 HMT activities have been identified. Each of these complexes contains the SET domain-containing homologs of yeast Set1, including human Set1 (hSet1), MLL1 (mixed lineage leukemia 1, also known as MLL, HRX, ALL1, or KMT2A), MLL2 (mixed-lineage leukemia 2, also known as HRX2 or KMT2B), MLL3 (mixed-lineage leukemia 3, also known as HALR or KMT2C), and MLL4 (mixed-lineage leukemia 4, also known as ALR or KMT2D), which carry the enzymatic activity for the associated complexes. | # |
|
L3MBTL1
(details) |
15905 | l(3)mbt-like 1 (Drosophila) | 26013 | Q9Y468 | LMBL1_HUMAN | MBT PF02820 310-377 417-484 521-586, zf-C2HC PF01530 622-650 | L3mbtl1 | 2676663 | A2A5N8 | LMBL1_MOUSE | ZC2HC, SAMD | Zinc fingers, C2HC-type containing, Sterile alpha motif (SAM) domain containing | Histone modification read | # | 18026117 | L3MBTL1 | histone | H1BK26, H4K20 | # | 18026117 | Crystal structures of the L3MBTL1 MBT repeats in complex with histone H4 peptides dimethylated on Lys20 (H4K20me2). Only the second of the three MBT repeats can bind mono- and dimethylated histone peptides. Its binding pocket has similarities to that of 53BP1 and is able to recognize the degree of histone lysine methylation. | # |
|
L3MBTL2
(details) |
18594 | l(3)mbt-like 2 (Drosophila) | 83746 | Q969R5 | LMBL2_HUMAN | zf-FCS_1 PF21319 87-118, MBT PF02820 214-286 327-390 432-503 540-604 | L3mbtl2 | 2443584 | P59178 | LMBL2_MOUSE | # | # | Histone modification read | # | 19233876 | RING2-L3MBTL2 | histone | H3K4, H3K9, H3K27, H4K20 | # | 19233876 | Methylation-state-specific recognition of histones by the MBT repeat protein L3MBTL2. | # |
|
L3MBTL3
(details) |
23035 | l(3)mbt-like 3 (Drosophila) | 84456 | Q96JM7 | LMBL3_HUMAN | MBT PF02820 268-335 375-441 479-544, SAM_1 PF00536 707-770 | L3mbtl3 | 2143628 | Q8BLB7 | LMBL3_MOUSE | SAMD | Sterile alpha motif (SAM) domain containing | Histone modification read | # | 23292653 | # | histone | H4K20me | # | 23292653 | Binds L3MBTL3 with a similar affinity to H4K20me histone | # |
|
L3MBTL4
(details) |
26677 | l(3)mbt-like 4 (Drosophila) | 91133 | Q8NA19 | LMBL4_HUMAN | MBT PF02820 88-155 196-263 300-366, zf-C2HC PF01530 379-407, SAM_1 PF00536 543-605 | L3mbtl4 | 2444889 | B1B1A0 | LMBL4_MOUSE | SAMD | Sterile alpha motif (SAM) domain containing | Histone modification read | # | 20698951 | # | histone | HKme | # | 20698951 | The L3MBTL4 protein contains three "malignant brain tumor" (MBT) domains. The MBT domain binds methylated histone residues. | # |
|
LAS1L
(details) |
25726 | LAS1-like (S. cerevisiae) | 81887 | Q9Y4W2 | LAS1L_HUMAN | Las1 PF04031 43-187 | Las1l | 1923380 | A2BE28 | LAS1L_MOUSE | # | # | Histone modification write cofactor, Histone modification write cofactor | Histone methylation, Histone acetylation | 20442285 | CHD8, MLL2/3, MLL4/WBP7 | histone | H3K4, H3,H4,H2A | H3K4me, H3K4me2, H3Ac, H4Ac, H2AAc | 15960975 | Facultative member of the MLL1/MLL complex. | # |
|
MASTL
(details) |
19042 | microtubule associated serine/threonine kinase-like | 84930 | Q96GX5 | GWL_HUMAN | Pkinase PF00069 36-188 736-835 | Mastl | 1914371 | Q8C0P0 | GWL_MOUSE | # | # | Histone modification write | Histone phosphorylation | 20818157 | # | histone | H1, H3 | H1p, H3p | 20818157 | Phosphorylates histone protein in vitro; however such activity is unsure in vivo (UniProt). | # |
|
MBNL1
(details) |
6923 | Muscleblind-like protein 1 (Triplet-expansion RNA-binding protein) | 4154 | Q9NR56 | MBNL1_HUMAN | zf-CCCH_2 PF14608 19-39, domain PF22628 48-86 216-253, zf-CCCH PF00642 183-205 | Mbnl1 | 1928482 | Q9JKP5 | MBNL1_MOUSE | ZC3H | Zinc fingers CCCH-type | RNA modification | Alternative splicing | 16946708, 19470458, 15257297 | # | RNA | mRNA | # | 16946708, 19470458, 15257297 | Regulates the TNNT2 exon 5 skipping through competition with U2AF2. Inhibits cardiac troponin-T (TNNT2) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion in muscle. Antagonistic regulator with CELF proteins. | New |
|
MBNL3
(details) |
20564 | Muscleblind-like protein 3 (Cys3His CCG1-required protein) (Muscleblind-like X-linked protein) (Protein HCHCR) | 55796 | Q9NUK0 | MBNL3_HUMAN | zf-CCCH_2 PF14608 20-40, domain PF22628 49-87 211-248, zf-CCCH_4 PF18044 179-200 | Mbnl3 | 2444912 | Q8R003 | MBNL3_MOUSE | ZC3H | Zinc fingers CCCH-type | RNA modification | Alternative splicing | 15257297 | # | RNA | mRNA | # | 15257297 | Inhibits cardiac troponin-T (TNNT2) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion in muscle. Antagonistic regulator with CELF proteins. | New |
|
MEN1
(details) |
7010 | multiple endocrine neoplasia I | # | O00255 | MEN1_HUMAN | Menin PF05053 4-499 550-610 | Men1 | 1316736 | O88559 | MEN1_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 14992727 | Menin-associated_HMT, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7 | histone | H3K4 | H3K4me | 14992727, 15199122 | Essential component of a MLL/SET1 histone methyltransferase (HMT) complex, a complex that specifically methylates 'Lys-4' of histone H3 (H3K4) (UniProt). | # |
|
METTL11B
(details) |
31932 | methyltransferase like 11B | 149281 | Q5VVY1 | NTM1B_HUMAN | Methyltransf_PK PF05891 65-278 | Mettl11b | 2685053 | B2RXM4 | NTM1B_MOUSE | METTL | Methyltransferase like | Histone modification writer | Histone methylation | 26543159 | # | protein | CENP-A | K55m | 26543159 | Regulates centromere function and mitosis | New |
|
METTL14
(details) |
29330 | methyltransferase like 14 | 57721 | Q9HCE5 | MET14_HUMAN | MT-A70 PF05063 186-363 | Mettl14 | 2442926 | Q3UIK4 | MET14_MOUSE | METTL | Methyltransferase like | RNA modification | RNA methylation | 24316715 | WMM | RNA | A of mRNA | m(6)A | 24316715 | Regulates mRNA stability, processing miRNA, DNA-reparation | New |
|
METTL16
(details) |
28484 | methyltransferase like 16 | 79066 | Q86W50 | MET16_HUMAN | Methyltransf_10 PF05971 1-291 | Mettl16 | 1914743 | Q9CQG2 | MET16_MOUSE | METTL | Methyltransferase like | RNA modification | RNA methylation | 29051200 | # | RNA | U6 snRNA (A43) | m6A43 | 32266935 | Tunes snRNA–pre‐mRNA interactions, controls alternative splicing | New |
|
METTL21A
(details) |
30476 | methyltransferase like 21A | 151194 | Q8WXB1 | MT21A_HUMAN | Methyltransf_16 PF10294 26-189 | Mettl21a | 1914349 | Q9CQL0 | MT21A_MOUSE | METTL | Methyltransferase like | Protein modification | Protein methylation | # | # | protein | Hsp70 | Km3 | 23921388 | Modulates the affinity of Hsp70 for targets | New |
|
METTL3
(details) |
17563 | methyltransferase like 3 | 56339 | Q86U44 | MTA70_HUMAN | MT-A70 PF05063 389-550 | Mettl3 | 1927165 | Q8C3P7 | MTA70_MOUSE | METTL | Methyltransferase like | RNA modification | RNA methylation | 24316715 | WMM | RNA | A of mRNA | m(6)A | 24316715 | Regulates mRNA stability, processing miRNA, DNA-reparation | New |
|
METTL4
(details) |
24726 | methyltransferase like 4 | 64863 | Q8N3J2 | METL4_HUMAN | MT-A70 PF05063 281-454 | Mettl4 | 1924031 | Q3U034 | METL4_MOUSE | METTL | Methyltransferase like | RNA modification, DNA modification | RNA methylation, DNA methylation | 30982744 | # | DNA, RNA | A of DNA, U2 snRNA | m(6)A | 31913360 | Regulates transcriptional silencing, Polycomb silencing, splicing regulation | New |
|
MINA
(details) |
19441 | MYC induced nuclear antigen | 84864 | Q8IUF8 | MINA_HUMAN | JmjC_2 PF08007 137-261, ROXA-like_wH PF20514 331-431 | Mina | 1914264 | Q8CD15 | MINA_MOUSE | # | # | Histone modification erase | Histone methylation | 19502796 | # | histone | H3K9me3 | H3K9 | 19502796 | mdig=MINA is involved in demethylation of tri-methyl lysine 9 on histone H3. | # |
|
MLLT1
(details) |
7134 | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 1 | 4298 | Q03111 | ENL_HUMAN | YEATS PF03366 27-107, AHD PF17793 496-555 | Mllt1 | 1927238 | # | # | # | # | Chromatin remodeling cofactor | # | 23623499 | SWI/SNF-like_EPAFa, SWI/SNF-like EPAFB | chromatin | # | # | 23623499 | MLL-ENL (=MLLT1) inhibits polycomb repressive complex 1. | # |
|
MORF4L1
(details) |
16989 | mortality factor 4 like 1 | 10933 | Q9UBU8 | MO4L1_HUMAN | Tudor-knot PF11717 11-52, MRG PF05712 175-351 | Morf4l1 | 1096551 | P60762 | MO4L1_MOUSE | # | # | Histone modification read | # | 21423274 | NuA4 | histone | H4 | # | 21423274 | Table 1 in reference (MRG15 =MORF4L1). | # |
|
MORF4L2
(details) |
16849 | mortality factor 4 like 2 | 9643 | Q15014 | MO4L2_HUMAN | MRG PF05712 101-280 | Morf4l2 | 1927167 | Q9R0Q4 | MO4L2_MOUSE | # | # | Histone modification erase cofactor | Histone acetylation | 12963728 | NuA4 | histone | # | # | 12963728 | The FLJ10914 protein is associated with components of the TRRAP/TIP60 histone acetyltransferase complex and binds directly to the MORF4-related MRG15 and MRGX proteins. | # |
|
MOV10
(details) |
7200 | Mov10 RISC complex RNA helicase | 4343 | Q9HCE1 | MOV10_HUMAN | MOV-10_N PF21632 15-85, MOV-10_Ig-like PF21633 119-240, Mov-10_helical PF21635 291-358, MOV-10_beta-barrel PF21634 358-448, AAA_11 PF13086 499-572 610-690, AAA_12 PF13087 699-921 | Mov10 | 97054 | P23249 | MOV10_MOUSE | # | # | # | # | 20543829 | # | histone | # | # | # | MOV10 may be directly involved in transcriptional silencing by PcG complexes. | # |
|
MST1
(details) |
7380 | macrophage stimulating 1 (hepatocyte growth factor-like) | 4485 | P26927 | HGFL_HUMAN | PAN_1 PF00024 26-104, Kringle PF00051 109-186 190-268 283-361 370-448, Trypsin PF00089 485-704 | Mst1 | 96080 | P26928 | HGFL_MOUSE | # | # | Histone modification | # | 17320507 | # | histone | # | # | # | Classified as histone-modifying enzymes in paper. | # |
|
MUM1
(details) |
29641 | melanoma associated antigen (mutated) 1 | 84939 | Q2TAK8 | MUM1_HUMAN | PWP3A-B_N PF20887 1-105, MUM1-like_PWWP PF20884 411-484, PWP3A-B_C PF20886 561-707 | Mum1 | 1915364 | Q6DID5 | MUM1_MOUSE | # | # | Histone modification read | # | 217205545 | # | histone | H3K36me, K3K79me, H4K20me | # | 217205545 | The PWWP domains in BRPF1, BRPF2, HDGF2, MUM1 and the N-terminal PWWP domains of WHSC1 and WHSC1L1 show weak binding affinity to histones with H3K36, K3K79 or H4K20 | # |
|
MYSM1
(details) |
29401 | Myb-like, SWIRM and MPN domains 1 | 114803 | Q5VVJ2 | MYSM1_HUMAN | Myb_DNA-binding PF00249 120-163, SWIRM PF04433 382-461, JAB PF01398 576-679 | Mysm1 | 2444584 | Q69Z66 | MYSM1_MOUSE | # | # | Histone modification erase | Histone ubiquitination | 17707232 | # | histone | H2Aub | H2A | 17707232 | JAMM/MPN(+) domain-containing histone H2A deubiquitinase (2A-DUB, or KIAA1915/MYSM1) is specific for monoubiquitinated H2A (uH2A) that has permitted delineation of a strategy for specific regulatory pathways of gene activation. | # |
|
NAP1L1
(details) |
7637 | nucleosome assembly protein 1-like 1 | 4673 | P55209 | NP1L1_HUMAN | NAP PF00956 77-344 | Nap1l1 | 1855693 | P28656 | NP1L1_MOUSE | # | # | Histone chaperone | # | 18226242 | # | histone | # | # | 18226242 | Human Nucleosome Assembly Protein-1 (hNAP-1) =NAP1L1 is known to act as a histone chaperone that shuttles histones H2A/H2B into the nucleus, assembles nucleosomes and promotes chromatin fluidity, thereby affecting transcription of several cellular genes. | # |
|
NAP1L2
(details) |
7638 | nucleosome assembly protein 1-like 2 | 4674 | Q9ULW6 | NP1L2_HUMAN | NAP PF00956 111-408 | Nap1l2 | 106654 | P51860 | NP1L2_MOUSE | # | # | Histone modification cofactor | # | 21333655, 17591696 | # | histone | H3, H4 | # | # | Interacts with H3 and H4 and may be involved in regulation of acetylation. | # |
|
NAP1L4
(details) |
7640 | nucleosome assembly protein 1-like 4 | 4676 | Q99733 | NP1L4_HUMAN | NAP PF00956 65-338 | Nap1l4 | 1316687 | Q78ZA7 | NP1L4_MOUSE | # | # | Histone modification cofactor | # | 21333655 | # | histone | H3, H4 | # | # | Interacts with H3 and H4 and may be involved in regulation of acetylation. | # |
|
NCOA6
(details) |
15936 | nuclear receptor coactivator 6 | 23054 | Q14686 | NCOA6_HUMAN | NCOA6_TRADD-N PF13820 47-182 | Ncoa6 | 1929915 | Q9JL19 | NCOA6_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 17500065 | CHD8, MLL2/3, COMPASS-like MLL3,4 | histone | # | # | 17500065 | Ectopically expressed PTIP is capable of interacting with DNA damage response proteins including 53BP1, while endogenous PTIP, and a novel protein PA1 are both components of a Set1-like histone methyltransferase (HMT) complex that also contains ASH2L, RBBP5, WDR5, hDPY-30, NCOA6, SET domain-containing HMTs MLL3 and MLL4, and substoichiometric amount of JmjC domain-containing putative histone demethylase UTX. | # |
|
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. | # |
|
NTMT1
(details) |
23373 | N-terminal Xaa-Pro-Lys N-methyltransferase 1 | 28989 | Q9BV86 | NTM1A_HUMAN | Methyltransf_PK PF05891 8-222 | Ntmt1 | 1913867 | Q8R2U4 | NTM1A_MOUSE | METTL | Methyltransferase like | Histone modification writer | Histone methylation | 26543159 | # | protein | CENP-A, CENP-B, RCC1 | Km1/m2/m3, Rm, Pm | 26543159 | Regulates centromere function and mitosis | New |
|
PAGR1
(details) |
28707 | PAXIP1 associated glutamate-rich protein 1 | 79447 | Q9BTK6 | PAGR1_HUMAN | PAXIP1_C PF15364 88-226 | 2900092E17Rik | 1914528 | Q99L02 | PAGR1_MOUSE | # | # | Histone modification write cofactor, Histone modification write cofactor | Histone methylation, Histone acetylation | 17500065 | CHD8, MLL2/3, MLL4/WBP7, COMPASS-like MLL3,4 | histone | # | # | 17500065 | Component of the MLL2/MLL3 complex (UniProt). | # |
|
PAXIP1
(details) |
8624 | PAX interacting (with transcription-activation domain) protein 1 | 22976 | Q6ZW49 | PAXI1_HUMAN | PTCB-BRCT PF12738 102-165 710-771, BRCT PF00533 604-684, RTT107_BRCT_5 PF16770 860-947, BRCT_2 PF16589 973-1062 | Paxip1 | 1890430 | Q6NZQ4 | PAXI1_MOUSE | # | # | Histone modification write cofactor | Histone methylation | 17178841 | CHD8, MLL2/3, MLL4/WBP7, COMPASS-like MLL3,4 | histone | H3K4 | H3K4me3 | 17178841 | ALR (MLL2) is a member of the human MLL family, which belongs to a larger SET1 family of histone methyltransferases. ALR is present within a stable multiprotein complex containing a cohort of proteins shared with other SET1 family complexes and several unique components, such as PTIP and the jumonji family member UTX. | # |
|
PCGF2
(details) |
12929 | polycomb group ring finger 2 | 7703 | P35227 | PCGF2_HUMAN | zf-C3HC4_2 PF13923 18-56, RAWUL PF16207 164-228 | Pcgf2 | 99161 | P23798 | PCGF2_MOUSE | RNF, PCGF | RING-type (C3HC4) zinc fingers, Polycomb group ring fingers | Polycomb group (PcG) protein | # | 21282530 | PRC1 | # | # | # | 21282530 | CBX7 and CBX8, two Polycomb (Pc) homologs that repress INK4a, both participate in PRC1-like complexes with at least two Posterior sex combs (Psc) proteins, MEL18 =PCGF2 and BMI1. | # |
|
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. | # |
|
PHF20L1
(details) |
24280 | PHD finger protein 20-like 1 | 51105 | A8MW92 | P20L1_HUMAN | Tudor_2 PF18104 90-124, PHD20L1_u1 PF16660 309-439, PHD_5 PF20826 675-729 | Phf20l1 | 2444412 | Q8CCJ9 | P20L1_MOUSE | TDRD, PHF | Tudor domain containing, Zinc fingers, PHD-type | Histone modification read | # | 21423274 | # | histone | H3K4me | # | 21423274 | Table 1 in the reference. Via its PWWP domain it specifically binds trimethylated 'Lys-36' of histone H3 (H3K36me3): early recruitment to chromatin to be replicated allowing a quick identification of mismatch repair to initiate the DNA mismatch repair rea | # |
|
PIWIL4
(details) |
18444 | piwi-like RNA-mediated gene silencing 4 | 143689 | Q7Z3Z4 | PIWL4_HUMAN | PAZ PF02170 272-405, Piwi PF02171 546-837 | Piwil4 | 3041167 | Q8CGT6 | PIWL4_MOUSE | AGO | Argonaute/PIWI family | Chromatin remodeling, Histone modification erase cofactor | Histone methylation | 17544373 | # | histone | H3K9 | # | 17544373 | Induced histone H3 lysine 9 methylation at the p16(Ink4a) (CDKN2A) locus. Suggests that PIWIL4 plays important roles in the chromatin-modifying pathway in human somatic cells. | # |
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PRMT2
(details) |
5186 | protein arginine methyltransferase 2 | 3275 | P55345 | ANM2_HUMAN | SH3_1 PF00018 36-82, MTS PF05175 131-210, domain PF22528 244-415 | Prmt2 | 1316652 | Q9R144 | ANM2_MOUSE | PRMT | Protein arginine methyltransferases | Histone modification write | Histone methylation | 19405910 | # | histone | H4 | H4me | 19405910 | PRMT2 activity is substantially lower than PRMT1 in vitro, but both enzymes selectively methylate histone H4 and PRMT2, like PRMT1, may act as a transcription co-activator through this modification. | # |
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PRMT8
(details) |
5188 | protein arginine methyltransferase 8 | 56341 | Q9NR22 | ANM8_HUMAN | PrmA PF06325 111-184, domain PF22528 217-380 | Prmt8 | 3043083 | Q6PAK3 | ANM8_MOUSE | PRMT | Protein arginine methyltransferases | Histone modification write | Histone methylation | 16051612 | # | histone | H4R | H4Rme | 16051612 | PRMT8 preferentially methylates histone H4 and the recombinant forms of GAR and Npl3, thus displaying PRMT1-like substrate specificity. | # |
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RAD54L
(details) |
9826 | RAD54-like (S. cerevisiae) | 8438 | Q92698 | RAD54_HUMAN | SNF2-rel_dom PF00176 156-462, Helicase_C PF00271 499-611 | Rad54l | 894697 | P70270 | RAD54_MOUSE | # | # | Chromatin remodeling | # | 8805304 | # | chromatin | # | # | 8805304 | V(D)J recombination does not involve homologous recombination, but mHR54 =RAD54L could mediate a substrate preparation step that V(D)J and meiotic recombination have in common, such as changing the chromatin structure of the loci that will be rearranged. | # |
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RAD54L2
(details) |
29123 | RAD54-like 2 (S. cerevisiae) | 23132 | Q9Y4B4 | ARIP4_HUMAN | SNF2-rel_dom PF00176 274-598, Helicase_C PF00271 725-854 | Rad54l2 | 1933196 | Q99NG0 | ARIP4_MOUSE | # | # | Chromatin remodeling | # | 19692572 | # | chromatin | # | # | 19692572 | ARIP4 =RAD54L2 contains SNF2 domain that functions as a motor protein in chromatin remodeling complexes. | # |
|
RAG1
(details) |
9831 | recombination activating gene 1 | 5896 | P15918 | RAG1_HUMAN | RAG1_imp_bd PF12560 1-291, zf-C3HC4 PF00097 293-331, zf-RAG1 PF10426 354-383, RAG1 PF12940 387-1022 | Rag1 | 97848 | P15919 | RAG1_MOUSE | RNF | RING-type (C3HC4) zinc fingers | Histone modification write | Histone ubiquitination | 21256161 | # | histone, DNA | H3.3K, DNA motif | H3.3Kub | 21256161 | It has been suggested that RAG1 targets H3.3, the H3 variant known to be associated with recombining loci, and thus most likely to be encountered by RAG1 during V(D)J recombination. This reaction is absolutely dependent on an intact RAG1 RING domain, and requires regions of the far N-terminus of RAG1 where the H3.3 binding sight is likely to reside and regions within the H3 amino-terminal tail. Several H3.3 lysines are subject to ubiquitylation. | # |
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RBBP4
(details) |
9887 | retinoblastoma binding protein 4 | 5928 | Q09028 | RBBP4_HUMAN | CAF1C_H4-bd PF12265 19-88, WD40 PF00400 173-206 221-256 265-302 309-346 367-402 | Rbbp4 | 1194912 | Q60972 | RBBP4_MOUSE | WDR | WD repeat domain containing | Histone chaperone | # | 8858152 | NuRF, SWI/SNF_Brg1(I), SWI/SNF_Brg1(II), SWI/SNF_Brm, NuRD, mSin3A, core HDAC, mSin3A-like complex, PRC2, CAF-1 | histone | H4 | # | 8858152 | RbAp46 and RbAp48 (pRB-associated proteins p46 and p48, also known as RBBP7 and RBBP4, respectively) are highly homologous histone chaperones that play key roles in establishing and maintaining chromatin structure. Human p48 =RBBP4 can bind to histone H4 in the absence of CAF-1 p150 and p60. p48, also a known subunit of a histone deacetylase, copurifies with a chromatin assembly complex (CAC), which contains the three subunits of CAF-1 (p150, p60, p48) and H3 and H4, and promotes DNA replication-dependent chromatin assembly. | # |
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RBBP5
(details) |
9888 | retinoblastoma binding protein 5 | 5929 | Q15291 | RBBP5_HUMAN | WD40 PF00400 29-52 62-94 | Rbbp5 | 1918367 | Q8BX09 | RBBP5_MOUSE | WDR | WD repeat domain containing | Histone modification write cofactor | Histone methylation | 19556245 | COMPASS, Menin-associated_HMT, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7, COMPASS-like MLL3,4 | histone | H3K4 | H3K4me1, H3K4me2, H3K4me3 | 19556245 | A five-component 200-kDa MLL1 core complex containing human MLL1, WDR5, RbBP5, Ash2L, and DPY-30. | # |
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RBBP7
(details) |
9890 | retinoblastoma binding protein 7 | 5931 | Q16576 | RBBP7_HUMAN | CAF1C_H4-bd PF12265 18-87, WD40 PF00400 172-205 220-255 264-301 308-345 366-402 | Rbbp7 | 1194910 | Q60973 | RBBP7_MOUSE | WDR | WD repeat domain containing | Histone chaperone | # | 18571423 | NuRF, NuRD, mSin3A, core HDAC, mSin3A-like complex, PRC2 | histone | H4 | # | 18571423 | RbAp46 and RbAp48 (pRB-associated proteins p46 and p48, also known as RBBP7 and RBBP4, respectively) are highly homologous histone chaperones that play key roles in establishing and maintaining chromatin structure. When a histone H3/H4 dimer (or tetramer) binds to RbAp46 or RbAp48, helix 1 of histone H4 unfolds to interact with the histone chaperone. | # |
|
RING1
(details) |
10018 | ring finger protein 1 | 6015 | Q06587 | RING1_HUMAN | zf-C3HC4_2 PF13923 47-87, RAWUL PF16207 282-400 | Ring1 | 1101770 | O35730 | RING1_MOUSE | RNF | RING-type (C3HC4) zinc fingers | Histone modification write, Polycomb group (PcG) protein | Histone ubiquitination | 15386022 | PRC1, BCOR, RING2-L3MBTL2, RING2-FBRS | histone | H2AK119 | H2AK119ub | 15386022 | The complex hPRC1L (human Polycomb repressive complex 1-like) is composed of several Polycomb-group proteins including Ring1, Ring2, Bmi1 and HPH2. hPRC1L monoubiquitinates nucleosomal histone H2A at lysine 119. | # |
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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. | # |
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RUVBL2
(details) |
10475 | RuvB-like AAA ATPase 2 | 10856 | Q9Y230 | RUVB2_HUMAN | TIP49 PF06068 21-364, TIP49_C PF17856 370-435 | Ruvbl2 | 1342299 | Q9WTM5 | RUVB2_MOUSE | INO80, AATP | INO80 complex subunits, ATPases / AAA-type | Chromatin remodeling cofactor | # | 18026119 | Ino80, SWR, NuA4, NuA4-related complex, CHD8, MLL2/3, MLL4/WBP7, SRCAP | chromatin | # | # | 18026119 | The seven human INO80 complex components include TIP49A and TIP49B (previously identified as ‘RuvB-like’ proteins, and labeled RUVBL1 and RUVBL2). | # |
|
SAP30
(details) |
10532 | Sin3A-associated protein, 30kDa | 8819 | O75446 | SAP30_HUMAN | zf-SAP30 PF13866 64-134, SAP30_Sin3_bdg PF13867 153-205 | Sap30 | 1929129 | O88574 | SAP30_MOUSE | # | # | Histone modification erase cofactor | Histone acetylation | 9651585 | mSin3A, mSin3A-like complex | histone | # | # | 9651585 | The human SAP30 complex is active in deacetylating core histone octamers. | # |
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SAP30L
(details) |
25663 | SAP30-like | 79685 | Q9HAJ7 | SP30L_HUMAN | zf-SAP30 PF13866 26-95, SAP30_Sin3_bdg PF13867 114-166 | Sap30l | 1354709 | Q5SQF8 | SP30L_MOUSE | # | # | Histone modification erase cofactor | Histone acetylation | 16820529 | # | histone | # | # | 16820529 | SAP30L induces transcriptional repression, possibly via recruitment of Sin3A and histone deacetylases. A functional nucleolar localization signal in SAP30L means that SAP30L and SAP30 are able to target Sin3A to the nucleolus. | # |
|
SCML2
(details) |
10581 | sex comb on midleg-like 2 (Drosophila) | 10389 | Q9UQR0 | SCML2_HUMAN | MBT PF02820 67-134 176-241, RBR PF17208 281-321, SLED PF12140 355-464, SAM_1 PF00536 628-695 | # | # | # | # | SAMD | Sterile alpha motif (SAM) domain containing | Polycomb group (PcG) protein | # | 24727478 | PRC1 | # | # | # | 24727478 | Scml2 is a member of the Polycomb group of proteins involved in epigenetic gene silencing. Human Scml2 is a part of a multisubunit protein complex, PRC1 (Polycomb repressive complex 1), which is responsible for maintenance of gene repression, prevention of chromatin remodeling, preservation of the "stemness" of the cell, and cell differentiation. | # |
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SCML4
(details) |
21397 | sex comb on midleg-like 4 (Drosophila) | 256380 | Q8N228 | SCML4_HUMAN | RBR PF17208 1-61, SLED PF12140 96-207, SAM_1 PF00536 343-410 | Scml4 | 2446140 | Q80VG1 | SCML4_MOUSE | SAMD | Sterile alpha motif (SAM) domain containing | Polycomb group (PcG) protein | # | # | # | # | # | # | # | Putative Polycomb group (PcG) protein. PcG proteins act by forming multiprotein complexes, which are required to maintain the transcriptionally repressive state of homeotic genes throughout development. (Annotated by similarity.) | # |
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SFMBT1
(details) |
20255 | Scm-like with four mbt domains 1 | 51460 | Q9UHJ3 | SMBT1_HUMAN | MBT PF02820 54-121 166-234 279-351 388-454, SLED PF12140 501-616, SAM_1 PF00536 793-857 | Sfmbt1 | 1859609 | Q9JMD1 | SMBT1_MOUSE | # | # | Polycomb group (PcG) protein | # | 21423274 | SCL | histone | H4K20 | # | 21423274 | Table 1 in the reference. | # |
|
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. | # |
|
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. | # |
|
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. | # |
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SMARCAL1
(details) |
11102 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 | 50485 | Q9NZC9 | SMAL1_HUMAN | HARP PF07443 245-304 344-397, SNF2-rel_dom PF00176 439-688, Helicase_C PF00271 714-822 | Smarcal1 | 1859183 | Q8BJL0 | SMAL1_MOUSE | # | # | Chromatin remodeling | # | 11799392 | # | chromatin | # | # | 11799392 | The unique constellation of findings constituting SIOD indicates that SMARCAL1 regulates the transcriptional activity of a particular subset of genes through chromatin remodeling during both development and later life. | # |
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SMARCB1
(details) |
11103 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 | 6598 | Q12824 | SNF5_HUMAN | INI1_DNA-bd PF21459 12-104, SNF5 PF04855 180-373 | Smarcb1 | 1328366 | Q9Z0H3 | SNF5_MOUSE | # | # | Histone modification read | # | 21423274 | 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 | histone | H3K56 | # | 21423274 | Table 1 in the reference (SMARCB1 =Snf5) | # |
|
SMARCC1
(details) |
11104 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 | 6599 | Q92922 | SMRC1_HUMAN | SWIRM-assoc_2 PF16496 31-165, SWIRM PF04433 459-537, Myb_DNA-binding PF00249 622-664, SWIRM-assoc_3 PF16498 705-772, SWIRM-assoc_1 PF16495 872-952 | Smarcc1 | 1203524 | P97496 | SMRC1_MOUSE | # | # | Chromatin remodeling cofactor | # | 10078207 | 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 | chromatin | # | # | 10078207 | The addition of INI1, BAF155 =SMARCC1, and BAF170 to BRG1 increases remodeling activity to a level comparable to that of the whole hSWI/SNF complex. | # |
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SMARCC2
(details) |
11105 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 | 6601 | Q8TAQ2 | SMRC2_HUMAN | SWIRM-assoc_2 PF16496 5-137, SWIRM PF04433 434-512, Myb_DNA-binding PF00249 600-642, SWIRM-assoc_3 PF16498 683-748, SWIRM-assoc_1 PF16495 864-945 | Smarcc2 | 1915344 | Q6PDG5 | SMRC2_MOUSE | # | # | Chromatin remodeling cofactor | # | 10078207 | 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 | chromatin | # | # | 10078207 | The addition of INI1, BAF155, and BAF170 =SMARCC2 to BRG1 increases remodeling activity to a level comparable to that of the whole hSWI/SNF complex. | # |
|
SMARCD1
(details) |
11106 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 | 6602 | Q96GM5 | SMRD1_HUMAN | SWIB PF02201 294-364 | Smarcd1 | 1933623 | Q61466 | SMRD1_MOUSE | # | # | Chromatin remodeling | # | 12917342 | BAF, nBAF, npBAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brm, SWI/SNF-like_EPAFa, WINAC, SWI/SNF-like EPAFB, SWI/SNF BRM-BRG1 | chromatin | # | # | 12917342 | BAF60a =SMARCD1 possesses at least two interaction surfaces, one for GR and BRG1 and a second for BAF155 and BAF170. A GR mutant, GR(R488Q), that fails to interact with BAF60a=SMARCD1 in vitro has reduced chromatin-remodeling activity and reduced transcriptional activity from the promoter assembled as chromatin in vivo. | # |
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SMARCD2
(details) |
11107 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 | 6603 | Q92925 | SMRD2_HUMAN | SWIB PF02201 310-379 | Smarcd2 | 1933621 | Q99JR8 | SMRD2_MOUSE | # | # | Chromatin remodeling cofactor | # | 20148946 | BAF, PBAF, SWI/SNF_Brg1(I), SWI/SNF_Brm, SWI/SNF-like EPAFB, bBAF, SWI/SNF BRM-BRG1 | chromatin | # | # | 20148946 | The SWI/SNF chromatin remodeling complexes are important regulators of transcription; they consist of large multisubunit assemblies containing either Brm or Brg1 as the catalytic ATPase subunit and a variable subset of approximately 10 Brg/Brm-associated factors (BAF). Among these factors, BAF60 proteins (BAF60a, BAF60b=SMARCD2 or BAF60c), which are found in most complexes, are thought to bridge interactions between transcription factors and SWI/SNF complexes. | # |
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SMARCE1
(details) |
11109 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 | 6605 | Q969G3 | SMCE1_HUMAN | HMG_box PF00505 66-134 | Smarce1 | 1927347 | O54941 | SMCE1_MOUSE | # | # | Chromatin remodeling cofactor | # | 12672490 | 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 | chromatin | # | # | 12672490 | In addition to Swi2/Snf2 proteins, there is evidence that other core components are required for chromatin-remodeling activity. More recently, two additional human Swi/Snf members, BAF57 =SMARCE1 and BAF60a, have been shown to interact directly with regulatory proteins. | # |
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SS18L1
(details) |
15592 | synovial sarcoma translocation gene on chromosome 18-like 1 | 26039 | O75177 | CREST_HUMAN | SSXT PF05030 12-73 | Ss18l1 | 2444061 | Q8BW22 | CREST_MOUSE | # | # | Chromatin remodeling | # | 23799466 | CREST-BRG1 | chromatin | # | # | 23799466 | - | # |
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SS18L2
(details) |
15593 | synovial sarcoma translocation gene on chromosome 18-like 2 | 51188 | Q9UHA2 | S18L2_HUMAN | SSXT PF05030 12-73 | Deb1 | 1349474 | Q9D174 | S18L2_MOUSE | # | # | Chromatin remodeling | # | 19163965, 8666667 | # | chromatin | # | # | 15986999 | # | # |
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SSRP1
(details) |
11327 | structure specific recognition protein 1 | 6749 | Q08945 | SSRP1_HUMAN | POB3_N PF17292 3-96, SSrecog PF03531 105-170, PH1_SSRP1-like PF21103 197-327, Rttp106-like_middle PF08512 340-427, HMG_box PF00505 547-615, SSRP1_C PF21092 663-709 | Ssrp1 | 107912 | Q08943 | SSRP1_MOUSE | # | # | Chromatin remodeling | # | 12934006 | FACT | histone | H3, H4 | # | 12934006 | Both FACT and Spt16 can bind to nucleosomes and H2A-H2B dimers, whereas SSRP1 can only bind to H3-H4 tetramers but not to intact nucleosomes. Possibly, upon FACT binding to the nucleosome in the transcribed region, Spt16 facilitates the H2A-H2B displacement, which promotes the interaction between SSRP1 and the “altered” nucleosome. | # |
|
SUPT16H
(details) |
11465 | suppressor of Ty 16 homolog (S. cerevisiae) | 11198 | Q9Y5B9 | SP16H_HUMAN | FACT-Spt16_Nlob PF14826 5-167, Peptidase_M24 PF00557 182-411, SPT16 PF08644 529-689, Rttp106-like_middle PF08512 809-895, SPT16_C PF21091 929-1031 | Supt16 | 1890948 | Q920B9 | SP16H_MOUSE | # | # | Histone modification read | # | 12934006 | WINAC, FACT | histone | H2A, H2B | # | 12934006 | Both FACT and Spt16=SUPT16H can bind to nucleosomes and H2A-H2B dimers, whereas SSRP1 can only bind to H3-H4 tetramers but not to intact nucleosomes. Possibly, upon FACT binding to the nucleosome in the transcribed region, Spt16 facilitates the H2A-H2B displacement, which promotes the interaction between SSRP1 and the “altered” nucleosome. | # |
|
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. | # |
|
TADA1
(details) |
30631 | transcriptional adaptor 1 | 117143 | Q96BN2 | TADA1_HUMAN | SAGA-Tad1 PF12767 7-107 136-193 | Tada1 | 1196415 | Q99LM9 | TADA1_MOUSE | # | # | Histone chaperone | # | 11564863 | STAGA | histone | H2A | # | 11564863 | Within STAGA are two novel histone fold-containing protein subunits: STAF65γ, which is encoded by the KIAA0764 gene of previously unknown function, and STAF42=TADA1, a novel histone H2A-like protein. | # |
|
TAF1L
(details) |
18056 | TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 210kDa-like | 138474 | Q8IZX4 | TAF1L_HUMAN | TBP-binding PF09247 26-86, DUF3591 PF12157 583-1047, zf-CCHC_6 PF15288 1278-1322, Bromodomain PF00439 1409-1488 1536-1612 | # | # | # | # | # | # | Histone modification read | # | 22464331 | # | histone | H1.4ac, H2Aac, H2Bac, H3ac, H4ac | # | 22464331 | Interacts (via bromo domains) with acetylated lysine residues on the N-terminus of histone H1.4, H2A, H2B, H3 and H4 (in vitro). | # |
|
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. | # |
|
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. | # |
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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. | # |
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TBL1XR1
(details) |
29529 | transducin (beta)-like 1 X-linked receptor 1 | 79718 | Q9BZK7 | TBL1R_HUMAN | LisH PF08513 6-32, WD40 PF00400 164-197 226-252 258-294 340-377 382-428 432-470 | Tbl1xr1 | 2441730 | Q8BHJ5 | TBL1R_MOUSE | WDR | WD repeat domain containing | # | # | 15601853 | # | histone | # | # | # | Targets Ncor repressive complex to deacethylated histones. | # |
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TLE1
(details) |
11837 | transducin-like enhancer of split 1 (E(sp1) homolog, Drosophila) | 7088 | Q04724 | TLE1_HUMAN | TLE_N PF03920 18-132, WD40 PF00400 477-511 531-558 577-602 607-644 692-725 739-766 | Tle1 | 104636 | Q62440 | TLE1_MOUSE | WDR | WD repeat domain containing | Chromatin remodeling, Histone modification cofactor | # | 9334241, 17041588 | # | histone | H3 | # | 9334241, 17041588 | Native Groucho/TLE proteins interact specifically with histone H3 and not with other core histones. | # |
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TLE2
(details) |
11838 | transducin-like enhancer of split 2 | 7089 | Q04725 | TLE2_HUMAN | TLE_N PF03920 18-130, WD40 PF00400 450-484 504-531 550-575 580-617 665-698 712-739 | Tle2 | 104635 | Q9WVB2 | TLE2_MOUSE | WDR | WD repeat domain containing | Histone modification cofactor | # | 17041588 | # | histone | H3 | H3K4, H3K9, H3K27me | 17041588 | CUL4-DDB1 complexes interact with multiple WD40-repeat proteins (WDRs) including TLE1-3, WDR5, L2DTL (also known as CDT2) and the Polycomb-group protein EED (also known as ESC). WDR5 and EED are core components of histone methylation complexes that are essential for histone H3 methylation and epigenetic control at K4 or K9 and K27, respectively. | # |
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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. | # |
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TLK1
(details) |
11841 | tousled-like kinase 1 | 9874 | Q9UKI8 | TLK1_HUMAN | Pkinase PF00069 458-734 | Tlk1 | 2441683 | Q8C0V0 | TLK1_MOUSE | # | # | Histone modification write | Histone phosphorylation | 11314006 | # | histone | H3S10 | H3S10ph | 11314006 | Purified TLK1B phosphorylates histone H3 at S(10) with high specificity both in a mix of core histones and in isolated chromatin, suggesting that histone H3 is a physiological substrate for TLK1B. | # |
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TLK2
(details) |
11842 | tousled-like kinase 2 | 11011 | Q86UE8 | TLK2_HUMAN | Pkinase PF00069 464-741 | Tlk2 | 1346023 | O55047 | TLK2_MOUSE | # | # | Histone modification write | Histone phosphorylation | 12660173 | # | chromatin | # | # | 12660173 | There is a functional co-operation between ATM and Chk1 in propagation of a checkpoint response during S phase, suggesting that, through transient inhibition of Tlk kinases, the ATM-Chk1-Tlk pathway may regulate processes involved in chromatin assembly. | # |
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TONSL
(details) |
7801 | tonsoku-like, DNA repair protein | 4796 | Q96HA7 | TONSL_HUMAN | TPR_8 PF13181 202-235, domain PF13176 311-344, Ank_2 PF12796 529-628, LRR_6 PF13516 1097-1120 1128-1151 1248-1271 | Tonsl | 1919999 | Q6NZL6 | TONSL_MOUSE | ANKRD | Ankyrin repeat domain containing | Chromatin remodeling | # | 21113133 | # | histone | # | # | 21113133 | Mms22L associates with Nfkbil2 =TONSL, which may function as a scaffolding unit to bridge chromatin to multiple protein complexes. | # |
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UHRF1
(details) |
12556 | ubiquitin-like with PHD and ring finger domains 1 | 29128 | Q96T88 | UHRF1_HUMAN | ubiquitin PF00240 2-75, TTD PF12148 133-285, PHD PF00628 318-363, SAD_SRA PF02182 417-585 | Uhrf1 | 1338889 | Q8VDF2 | UHRF1_MOUSE | RNF | RING-type (C3HC4) zinc fingers | Histone modification read, Histone modification write cofactor | Histone ubiquitination | 17967883 | # | histone, DNA | H3K9me3, H3R2, H3, mCG | H3ub | 17967883 | ICBP90 =UHRF1and its murine homologue Np95 are enriched in pericentric heterochromatin of interphase nuclei, and this localization is dependent on H3K9 methylation. | # |
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UHRF2
(details) |
12557 | ubiquitin-like with PHD and ring finger domains 2, E3 ubiquitin protein ligase | 115426 | Q96PU4 | UHRF2_HUMAN | ubiquitin PF00240 2-74, TTD PF12148 125-311, PHD PF00628 347-392, SAD_SRA PF02182 445-614 | Uhrf2 | 1923718 | Q7TMI3 | UHRF2_MOUSE | RNF, PHF | RING-type (C3HC4) zinc fingers, Zinc fingers, PHD-type | Histone modification read | # | 15361834 | # | histone, DNA | H3K9me3, mCG | # | 15361834 | The SRA domain of the murine homologue of ICBP90=UHRF2, Np95, has histone H3-binding activity (Citterio et al., 2004). Methylated DNA twisted around histone H3 might be the primary target for Np95 and ICBP90 in vivo. | # |
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USP17L2
(details) |
34434 | ubiquitin specific peptidase 17-like family member 2 | 377630 | Q6R6M4 | U17L2_HUMAN | UCH PF00443 81-372 | Usp17le | 3643640 | Q7M764 | U17PE_MOUSE | # | # | Histone modification erase cofactor | Histone ubiquitination | 21239494 | # | histone | # | # | 21239494 | SDS3 is a key component of the histone deacetylase (HDAC)-dependent Sin3A co-repressor complex, serving to maintain its HDAC activity. Both exogenous and endogenous functional interaction between deubiquitinating enzyme USP17 = USP17L2 and human SDS3 has been reported. | # |
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USP44
(details) |
20064 | ubiquitin specific peptidase 44 | 84101 | Q9H0E7 | UBP44_HUMAN | zf-UBP PF02148 28-91, UCH PF00443 273-675 | Usp44 | 3045318 | Q8C2S0 | UBP44_MOUSE | USP | Ubiquitin-specific peptidases | Histone modification erase | Histone ubiquitination | 22681888 | # | histone | H2Bub1 | H2B | 22681888 | USP44 is most likely an H2Bub1-specific DUB, whose downregulation during ESC differentiation contributes to increased H2Bub1 levels. | # |
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VIRMA
(details) |
24500 | Protein virilizer homolog | 25962 | Q69YN4 | VIR_HUMAN | VIR_N PF15912 5-278 | Virma | 1913435 | A2AIV2 | VIR_MOUSE | ARMH | Armadillo like helical domain containing | RNA modification | RNA methylation | 29507755 | WMM | RNA | A of mRNA | m6A | 29507755 | Mediates methylation in 3'UTR and near stop codon | New |
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VPS72
(details) |
11644 | vacuolar protein sorting 72 homolog (S. cerevisiae) | 6944 | Q15906 | VPS72_HUMAN | YL1 PF05764 7-212, YL1_C PF08265 291-319 | Vps72 | 1202305 | Q62481 | VPS72_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 14966270 | NuA4, NuA4-related complex | chromatin | # | # | 14966270 | The YL1 =VPS72 protein is a subunit of the TRRAP/TIP60 HAT complex. The YL1 protein is also present in cells as a subunit of the previously uncharacterized mammalian SRCAP complex, which bears a striking similarity to the S. cerevisiae SWR1 chromatin remodeling complex. | # |
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WDR5
(details) |
12757 | WD repeat domain 5 | 11091 | P61964 | WDR5_HUMAN | WD40 PF00400 38-72 78-115 119-157 161-199 203-242 246-287 292-331 | Wdr5 | 2155884 | P61965 | WDR5_MOUSE | WDR | WD repeat domain containing | Histone modification read | # | 16946699 | ATAC, NSL, RING2-L3MBTL2, COMPASS, Menin-associated_HMT, MLL-HCF, CHD8, MLL2/3, COMPASS-like MLL1,2, MLL4/WBP7, COMPASS-like MLL3,4 | histone | H3K4, H3K4me1, H3K4me2, H3K4me3 | # | 16946699 | The WD40 domain of WDR5 represents a new class of histone methyl-lysine recognition domains that is important for recruiting H3K4 methyltransferases to K4-dimethylated histone H3 tail as well as for global and gene-specific K4 trimethylation. Here is given the crystal structures of full-length WDR5, WDR5Delta23 and its complexes with unmodified, mono-, di- and trimethylated histone H3K4 peptides. | # |
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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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WSB2
(details) |
19222 | WD repeat and SOCS box containing 2 | 55884 | Q9NYS7 | WSB2_HUMAN | WD40 PF00400 145-182 188-225 231-267 289-320 338-360, SOCS_box PF07525 367-401 | Wsb2 | 2144041 | O54929 | WSB2_MOUSE | WDR | WD repeat domain containing | Histone modification write | Histone ubiquitination | 21070969 | # | histone | # | # | # | May be a substrate-recognition component of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins, including histones. (Annotated by similarity). | # |
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ZNHIT1
(details) |
21688 | zinc finger, HIT-type containing 1 | 10467 | O43257 | ZNHI1_HUMAN | zf-HIT PF04438 113-141 | Znhit1 | 1917353 | Q8R331 | ZNHI1_MOUSE | ZNHIT | Zinc fingers, HIT-type | Chromatin remodeling cofactor, Histone modification erase cofactor | Histone acetylation | 15647280 | SRCAP | histone | # | # | 15647280 | YL1 protein is also present in cells as a subunit of the previously uncharacterized mammalian SRCAP complex, which bears a striking similarity to the recently described S. cerevisiae SWR1 chromatin remodeling complex and is composed of the SNF2-related SRCAP helicase, ARP6, ZnF/HIT1. | # |
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ZRANB3
(details) |
25249 | zinc finger, RAN-binding domain containing 3 | 84083 | Q5FWF4 | ZRAB3_HUMAN | SNF2-rel_dom PF00176 40-299, Helicase_C PF00271 329-435, zf-RanBP PF00641 623-648, HNH PF01844 1014-1049 | Zranb3 | 1918362 | Q6NZP1 | ZRAB3_MOUSE | ZRANB | Zinc fingers, RAN-binding domain containing | Chromatin remodeling, Histone modification read cofactor | Histone methylation | 22705370 | # | histone | # | # | 22705370 | All four proteins (HARP, HARP-like domain (HPL), SMARCA1, RAD54L) belong to the SNF2 =ZRANB3 family, whose members participate in a variety of processes including chromatin remodeling, transcription, DNA repair, and recombination. | # |