| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
ANP32A
(details) |
13233 | acidic (leucine-rich) nuclear phosphoprotein 32 family, member A | 8125 | P39687 | AN32A_HUMAN | LRR_9 PF14580 52-146 | Anp32a | 108447 | O35381 | AN32A_MOUSE | ANP32 | ANP32 acidic nuclear phosphoproteins | Chromatin remodeling cofactor | # | 11163245 | # | chromatin | # | # | 11163245 | pp32 = ANP32A is a member of a family of leucine-rich acidic nuclear proteins ( 7 and 19). Results suggest potential roles of INHAT subunits in chromatin remodeling and transcriptional regulation; INHAT complex including pp32 inhibits the HAT activity of p300/CBP and PCAF by binding to their substrate, histones. | # |
|
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. | # |
|
BRD2
(details) |
1103 | bromodomain containing 2 | 6046 | P25440 | BRD2_HUMAN | Bromodomain PF00439 85-167 354-440, BET PF17035 640-704 | Brd2 | 99495 | Q7JJ13 | BRD2_MOUSE | # | # | Histone modification read | # | 18406326, 20495584 | # | histone | H3K9me2, H3K14me2, H4K5ac, H4K12ac, H3K27ac | # | 18406326, 20495584 | Brd2- and Brd3-associated chromatin is significantly enriched in H4K5, H4K12, and H3K14 acetylation and contains relatively little dimethylated H3K9. Both Brd2 and Brd3 allowed RNA polymerase II to transcribe through nucleosomes in a defined transcription system. Such activity depended on specific histone H4 modifications known to be recognized by the Brd proteins.. BRD2 is involved in recognizing acetylated lysines, including H3K27ac, and its involvement in transcriptional regulation. | # |
|
CDK9
(details) |
1780 | cyclin-dependent kinase 9 | 1025 | P50750 | CDK9_HUMAN | Pkinase PF00069 19-315 | Cdk9 | 1328368 | Q99J95 | CDK9_MOUSE | CDK | Cyclin-dependent kinases | Histone modification cofactor | # | 19844166 | # | histone | # | # | # | CDK9 functions to guide a complex network of chromatin modifications including histone H2B monoubiquitination (H2Bub1), H3 lysine 4 trimethylation (H3K4me3) and H3K36me3. UniProt: Protein kinase involved in the regulation of transcription. Part of the complex P-TEFb involved in cotranscriptional histone modification. | # |
|
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). | # |
|
EXOSC1
(details) |
17286 | exosome component 1 | 51013 | Q9Y3B2 | EXOS1_HUMAN | ECR1_N PF14382 8-43, EXOSC1 PF10447 95-135 | Exosc1 | 1913833 | Q9DAA6 | EXOS1_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC2
(details) |
17097 | exosome component 2 | 23404 | Q13868 | EXOS2_HUMAN | ECR1_N PF14382 26-64, RRP4_S1 PF21266 75-146, KH_6 PF15985 169-210 | Exosc2 | 2385133 | Q8VBV3 | EXOS2_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC3
(details) |
17944 | exosome component 3 | 51010 | Q9NQT5 | EXOS3_HUMAN | RRP40_N_mamm PF21261 26-106, RRP40_S1 PF21262 108-191, KH_6 PF15985 197-244 | Exosc3 | 1913612 | Q7TQK4 | EXOS3_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC4
(details) |
18189 | exosome component 4 | 54512 | Q9NPD3 | EXOS4_HUMAN | RNase_PH PF01138 21-152, RNase_PH_C PF03725 155-219 | Exosc4 | 1923576 | Q921I9 | EXOS4_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC5
(details) |
24662 | exosome component 5 | 56915 | Q9NQT4 | EXOS5_HUMAN | RNase_PH PF01138 28-147, RNase_PH_C PF03725 151-215 | Exosc5 | 107889 | Q9CRA8 | EXOS5_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC6
(details) |
19055 | exosome component 6 | 118460 | Q5RKV6 | EXOS6_HUMAN | RNase_PH PF01138 37-175 | Exosc6 | 1919794 | Q8BTW3 | EXOS6_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC7
(details) |
28112 | exosome component 7 | 23016 | Q15024 | EXOS7_HUMAN | RNase_PH PF01138 32-166, RNase_PH_C PF03725 196-261 | Exosc7 | 1913696 | Q9D0M0 | EXOS7_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC8
(details) |
17035 | exosome component 8 | 11340 | Q96B26 | EXOS8_HUMAN | RNase_PH PF01138 31-166, RNase_PH_C PF03725 192-257 | Exosc8 | 1916889 | Q9D753 | EXOS8_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
EXOSC9
(details) |
9137 | exosome component 9 | 5393 | Q06265 | EXOS9_HUMAN | RNase_PH PF01138 32-163, RNase_PH_C PF03725 189-254 | Exosc9 | 1355319 | Q9JHI7 | EXOS9_MOUSE | # | # | Scaffold protein, RNA modification | RNA degradation | 17174896 | RNA exosome | RNA | # | # | 17174896 | RNA abundance is regulated by balancing transcription and RNA degradation, processes that control the temporal and spatial distribution of cellular RNA. After decapping, 5′ to 3′ RNA degradation is accomplished by Xrn1, a 5′ to 3′ exoribonuclease. In the 3′ to 5′ pathway, RNA degradation is catalyzed by a multisubunit 3′ to 5′ exoribonuclease complex termed the RNA exosome. Three additional exosome subunits, Csl4=EXOSC1, Rrp4=EXOSC2, and Rrp40=EXOSC3, include S1 or KH domains, which are postulated to bind RNA. | # |
|
GLYR1
(details) |
24434 | glyoxylate reductase 1 homolog (Arabidopsis) | 84656 | Q49A26 | GLYR1_HUMAN | PWWP PF00855 8-89, NAD_binding_2 PF03446 269-425, NAD_binding_11 PF14833 431-551 | Glyr1 | 1921272 | Q922P9 | GLYR1_MOUSE | # | # | Histone modification read | # | 20850016 | # | histone | H3K4me3 | # | 20850016 | N-PAC=GLYR1, MSH-6, and NSD1 as well as NSD2 were identified as H3K36me3 interactors (Figure 1C; Table S2). Interestingly, these four proteins share a PWWP domain which is part of the Tudor domain “Royal Family” and includes the Tudor, chromo and MBT domains that can interact with methylated lysine residues. | # |
|
HNRPL
(details) |
5045 | Heterogeneous nuclear ribonucleoprotein L (hnRNP L) | 3191 | P14866 | HNRPL_HUMAN | RRM_1 PF00076 106-155, RRM_8 PF11835 191-269, RRM_5 PF13893 361-480, domain PF22976 492-587 | Hnrpl | 104816 | Q8R081 | HNRPL_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 25623890 | # | RNA | mRNA | # | 25623890 | Regulates exon inclusion of CD44 | New |
|
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. | # |
|
KDM5D
(details) |
11115 | lysine (K)-specific demethylase 5D | 8284 | Q9BY66 | KDM5D_HUMAN | JmjN PF02375 15-48, ARID PF01388 81-165, PHD PF00628 317-361, JmjC PF02373 491-607, KDM5_C-hel PF21323 611-665, zf-C5HC2 PF02928 697-749, PLU-1 PF08429 763-1085 | Kdm5d | 99780 | Q62240 | KDM5D_MOUSE | KDM, PHF | Chromatin-modifying enzymes / K-demethylases, Zinc fingers, PHD-type | Histone modification erase | Histone methylation | 17320160 | # | histone | H3K4me3, H3K4me2 | H3K4 | 17320160 | SMCX family members, including SMCY=KDM5D, RBP2, and PLU-1, demethylate H3K4me3. | # |
|
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. | # |
|
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 |
|
NAA60
(details) |
25875 | N(alpha)-acetyltransferase 60, NatF catalytic subunit | 79903 | Q9H7X0 | NAA60_HUMAN | Acetyltransf_1 PF00583 27-155 | Naa60 | 1922013 | Q9DBU2 | NAA60_MOUSE | NAA | N(alpha)-acetyltransferase subunits | Histone modification write | Histone acetylation | 21981917 | # | histone | H4K20, H4K79, H4K91 | H4K20ac, H4K79ac, H4K91ac | 21981917 | HAT4 =NAA60 is localized in the Golgi apparatus and displays a substrate preference for lysine residues of free histone H4, including H4K79 and H4K91, that reside in the globular domain of H4. | # |
|
NCL
(details) |
7667 | nucleolin | 4691 | P19338 | NUCL_HUMAN | RRM_1 PF00076 309-377 395-459 488-554 574-641 | Ncl | 97286 | P09405 | NUCL_MOUSE | RBM | RNA binding motif (RRM) containing | Histone chaperone | # | 16601700 | # | histone, DNA, RNA | DNA motif, RNA motif | # | 16601700, 15371412 | The nuclear protein nucleolin =NCL possesses a histone chaperone activity and this factor greatly enhances the activity of the chromatin remodeling machineries SWI/SNF and ACF. | # |
|
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. | # |
|
PPARGC1A
(details) |
9237 | peroxisome proliferator-activated receptor gamma, coactivator 1 alpha | 10891 | Q9UBK2 | PRGC1_HUMAN | RRM_1 PF00076 679-739 | Ppargc1a | 1342774 | O70343 | PRGC1_MOUSE | RBM | RNA binding motif (RRM) containing | Histone modification cofactor | # | 10558993 | # | histone | # | # | # | PPARgamma coactivator-1 (PGC-1) promotes transcription through the assembly of a complex that includes the histone acetyltransferases steroid receptor coactivator-1 (SRC-1). Promotes transcription through the assembly of a complex that includes HAT p300. | # |
|
PPP4R2
(details) |
18296 | protein phosphatase 4, regulatory subunit 2 | 151987 | Q9NY27 | PP4R2_HUMAN | PPP4R2 PF09184 5-309 | Ppp4r2 | 3027896 | Q0VGB7 | PP4R2_MOUSE | PPP4R | Serine/threonine phosphatases / Protein phosphatase 4, regulatory subunits | Histone modification cofactor | # | 18614045 | PPP4C-PPP4R2-PPP4R3A | histone | # | # | # | Regulatory subunit of serine/threonine-protein phosphatase 4 (PP4) complex. PPARgamma coactivator-1 (PGC-1) promotes transcription through the assembly of a complex that includes the histone acetyltransferases steroid receptor coactivator-1 | # |
|
RBFOX1
(details) |
9910 | RNA-binding motif protein, X chromosome (Glycoprotein p43) (Heterogeneous nuclear ribonucleoprotein G) (hnRNP G) [Cleaved into: RNA-binding motif protein, X chromosome, N-terminally processed] | 27316 | P38159 | RBMX_HUMAN | RRM_1 PF00076 10-80, RBM1CTR PF08081 169-221 | Rbmx | 1343044 | Q9WV02 | RBMX_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 12165565 | # | RNA | mRNA | # | 12165565 | Promotes exon 7 inclusion of SMN | New |
|
RBM24
(details) |
21539 | RNA-binding protein 24 (RNA-binding motif protein 24) (RNA-binding region-containing protein 6) | 221662 | Q9BX46 | RBM24_HUMAN | RRM_1 PF00076 13-70 | Rbm24 | 3610364 | D3Z4I3 | RBM24_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 29104163, 26990106 | # | RNA | mRNA | # | 29104163, 26990106 | Promotes alternative splicing events of several pluripotency and/or differentiation genes. Mediates preferentially muscle-specific exon inclusion in numerous mRNAs important for striated cardiac and skeletal muscle cell differentiation | New |
|
RFOX1
(details) |
18222 | RNA binding protein fox-1 homolog 1 (Ataxin-2-binding protein 1) (Fox-1 homolog A) (Hexaribonucleotide-binding protein 1) | 54715 | Q9NWB1 | RFOX1_HUMAN | RRM_1 PF00076 120-186, Fox-1_C PF12414 254-342 | Rbfox1 | 1926224 | Q9JJ43 | RFOX1_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 16537540 | # | RNA | mRNA | # | 16537540 | Activates inclusion of 4.1R exon 16 | New |
|
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. | # |
|
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). | # |
|
SETD1A
(details) |
29010 | SET domain containing 1A | 9739 | O15047 | SET1A_HUMAN | RRM_1 PF00076 97-166, N-SET PF11764 1419-1559, SET PF00856 1580-1685 | Setd1a | 2446244 | # | # | KMT, RBM | Chromatin-modifying enzymes / K-methyltransferases, RNA binding motif (RRM) containing | Histone modification write | Histone methylation | 17355966 | COMPASS | histone | H3K4 | H3K4me | 17355966 | The CFP1 complex contains human homologues of the COMPASS complex, including Set1A=SETD1A, Wdr5, Ash2, Rbbp5, and Wdr82 (previously denoted hSwd2). The human Set1A-CFP1 complex exhibits histone H3-Lys4 methyltransferase activity in vitro. | # |
|
SETD6
(details) |
26116 | SET domain containing 6 | 79918 | Q8TBK2 | SETD6_HUMAN | SET PF00856 75-286, Rubis-subs-bind PF09273 328-465 | Setd6 | 1913333 | Q9CWY3 | SETD6_MOUSE | # | # | Chromatin remodeling, Histone modification write | Histone methylation | 21131967 | # | histone | # | # | 21131967 | SETD6 monomethylation of nuclear RelA at K310 attenuates NF-κB signaling by docking GLP (via its ankyrin repeats) at target genes to generate a silent chromatin state, effectively rendering chromatin-bound RelA inert. As deregulation of NF-κB is linked to pathologic inflammatory processes and cancer8 and SETD6 inhibits NF-κB signaling in diverse cell types, including primary human cells, SETD6 may provide a new link by which protein lysine methylation and chromatin regulation influence tumor suppression and anti-inflammatory respons. | # |
|
SF3B1
(details) |
10768 | splicing factor 3b, subunit 1, 155kDa | 23451 | O75533 | SF3B1_HUMAN | SF3b1 PF08920 327-453, domain PF22646 1086-1158 | Sf3b1 | 1932339 | Q99NB9 | SF3B1_MOUSE | # | # | RNA modification | # | 23568491 | B-WICH | RNA | # | # | 23568491 | Although the causative link between SF3B1 mutation and CLL pathogenesis remains unclear, several lines of evidence suggest SF3B1 mutation might be linked to genomic stability and epigenetic modification. | # |
|
SKP1
(details) |
10899 | S-phase kinase-associated protein 1 | 6500 | P63208 | SKP1_HUMAN | Skp1_POZ PF03931 3-68, Skp1 PF01466 113-160 | Akp1a | 103575 | Q9WTX5 | SKP1_MOUSE | # | # | Histone modification write cofactor | Histone ubiquitination | 16943429 | BCOR | histone | # | # | 16943429 | The proteins in the BCOR complex include the PcG and PcG-associated proteins NSPC1, RING1, RNF2, and RYBP as well as components of an SCF ubiquitin ligase, SKP1, and FBXL10. BCOR recruits a unique combination of enzymatic activities to chromatin targets: a PcG E3 ubiquitin ligase for histone H2A, a demethylase for histone H3 K36, and an SCF E3 ubiquitin ligase. | # |
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SPEN
(details) |
17575 | spen family transcriptional repressor | 23013 | Q96T58 | MINT_HUMAN | RRM_1 PF00076 8-67 337-407 439-508 519-583, MINT_MID PF20809 2012-3467, MINT_RID PF20810 2366-2584 3009-3469, MINT_RAM7 PF20808 2654-2749, SPOC PF07744 3506-3662 | Spen | 1891706 | Q62504 | MINT_MOUSE | RBM | RNA binding motif (RRM) containing | Histone modification erase cofactor, TF | Histone acetylation, TF activator, TF repressor | 11331609 | # | histone | # | # | 11331609 | SHARP =SPEN recruits histone deacetylase activity. SHARP is a potent transcriptional repressor whose repression domain (RD) interacts directly with SMRT and at least five members of the NuRD complex including HDAC1 and HDAC2. | # |
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SRSF6
(details) |
10788 | Serine/arginine-rich splicing factor 6 (Pre-mRNA-splicing factor SRP55) (Splicing factor, arginine/serine-rich 6) | 6431 | Q13247 | SRSF6_HUMAN | RRM_1 PF00076 4-64 112-177 | Srsf6 | 1915246 | Q3TWW8 | SRSF6_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 22767602 | # | RNA | mRNA | # | 22767602 | Promotes Tau exon 10 inclusion | New |
|
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. | # |
|
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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TET1
(details) |
29484 | tet methylcytosine dioxygenase 1 | 80312 | Q8NFU7 | TET1_HUMAN | zf-CXXC PF02008 585-625, Tet_JBP PF12851 1580-2051 | Tet1 | 1098693 | Q3URK3 | TET1_MOUSE | # | # | DNA modification | DNA hydroxymethylation | 23222540 | # | DNA | mC | hmC | 23222540 | Ten eleven translocation (TET) enzymes, including TET1, TET2 and TET3, convert 5-methylcytosine to 5-hydroxymethylcytosine and regulate gene transcription. | # |
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TET2
(details) |
25941 | tet methylcytosine dioxygenase 2 | 54790 | Q6N021 | TET2_HUMAN | Tet_JBP PF12851 1290-1904 | Tet2 | 2443298 | Q4JK59 | TET2_MOUSE | # | # | DNA modification | DNA hydroxymethylation | 23222540 | # | DNA | mC | hmC | 23222540 | Ten eleven translocation (TET) enzymes, including TET1, TET2 and TET3, convert 5-methylcytosine to 5-hydroxymethylcytosine and regulate gene transcription. Downregulation of TET2 reduces the amount of histone 2B Ser 112 GlcNAc marks in vivo, which are associated with gene transcription regulation. | # |
|
TET3
(details) |
28313 | tet methylcytosine dioxygenase 3 | 200424 | O43151 | TET3_HUMAN | zf-CXXC PF02008 52-90, Tet_JBP PF12851 986-1697 | Tet3 | 2446229 | Q8BG87 | TET3_MOUSE | # | # | DNA modification | DNA hydroxymethylation | 23222540 | # | DNA | mC | hmC | 23222540 | Ten eleven translocation (TET) enzymes, including TET1, TET2 and TET3, convert 5-methylcytosine to 5-hydroxymethylcytosine and regulate gene transcription. There is a direct interaction of TET2 and TET3 with O-GlcNAc transferase (OGT). | # |
|
TFPT
(details) |
13630 | TCF3 (E2A) fusion partner (in childhood Leukemia) | 29844 | P0C1Z6 | TFPT_HUMAN | Tfpt | 1916964 | Q3U1J1 | TFPT_MOUSE | INO80 | INO80 complex subunits | Chromatin remodeling cofactor, DNA modification | DNA hydroxymethylation | 16230350 | Ino80 | chromatin | # | # | 16230350 | Subunit Composition of the hINO80 Complex: These proteins included the “Pim-1 kinase-associated protein-associated protein 1” (PAPA-1, GI 13775202), Amida (also known as TCF3 =TFPT). | # | |
|
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. | # |
|
TRA2B
(details) |
10781 | Transformer-2 protein homolog beta (TRA-2 beta) (TRA2-beta) (hTRA2-beta) (Splicing factor, arginine/serine-rich 10) (Transformer-2 protein homolog B) | 6434 | P62995 | TRA2B_HUMAN | RRM_1 PF00076 122-190 | Tra2B | 106016 | P62996 | TRA2B_MOUSE | RBM | RNA binding motif containing | RNA modification | Alternative splicing | 12165565 | # | RNA | mRNA | # | 12165565 | Promotes exon 7 inclusion of SMN | New |
|
TRRAP
(details) |
12347 | transformation/transcription domain-associated protein | 8295 | Q9Y4A5 | TRRAP_HUMAN | Tra1_central PF20175 240-895, Tra1_ring PF20206 1003-2695, FAT PF02259 2851-3201, PI3_PI4_kinase PF00454 3531-3782 | Trrap | 2153272 | Q80YV3 | TRRAP_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 14966270 | SWR, PCAF, TFTC-HAT, NuA4, SAGA, NuA4-related complex, STAGA | histone | # | # | 14966270 | The complex(es) contain(s) other subunits shared with NuA4, including TRRAP, p400/hDomino, Brd8. | # |
|
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). | # |
|
YEATS4
(details) |
24859 | YEATS domain containing 4 | 8089 | O95619 | YETS4_HUMAN | YEATS PF03366 42-121 | Yeats4 | 1927224 | Q9CR11 | YETS4_MOUSE | # | # | Histone modification write cofactor | Histone acetylation | 14966270 | NuA4, NuA4-related complex, SRCAP | histone | # | # | 14966270 | The essential GAS41 =YEATS4 protein is a member of the AF9/ENL-related (YEATS) family, and associated to transcription/chromatin-modifying complexes, including yeast NuA4, NuA3, Sas2, SWI/SNF, TFIID/mediator/TFIIF, and human SWI/SNF complexes. | # |
|
ZMYM2
(details) |
12989 | zinc finger, MYM-type 2 | 7750 | Q9UBW7 | ZMYM2_HUMAN | zf-FCS PF06467 328-364 371-412 422-457 465-504 534-571 637-674 681-716 725-762 766-803, DUF3504 PF12012 1190-1359 | Zmym2 | 1923257 | Q9CU65 | ZMYM2_MOUSE | ZMYM | Zinc fingers, MYM type | Histone modification erase cofactor, TF | Histone acetylation | 12493763 | BHC, LSD-CoREST | DNA | DNA motif | # | 12493763 | A family of HDAC1,2-associated complexes includes proteins with a putative role in DNA binding such as ZNF261/XFIM (=ZMYM3), ZNF198/FIM (=ZMYM2), and ZNF217. | # |
|
ZMYM3
(details) |
13054 | zinc finger, MYM-type 3 | 9203 | Q14202 | ZMYM3_HUMAN | zf-FCS PF06467 353-389 406-444 449-490 497-535 546-580 591-624 632-664 676-714 718-754, DUF3504 PF12012 1184-1354 | Zmym3 | 1927231 | Q9JLM4 | ZMYM3_MOUSE | ZMYM | Zinc fingers, MYM type | Histone modification erase cofactor | Histone acetylation | 12493763 | BHC | DNA | # | # | 12493763 | A family of HDAC1,2-associated complexes includes proteins with a putative role in DNA binding such as ZNF261/XFIM (=ZMYM3), ZNF198/FIM (=ZMYM2), and ZNF217. | # |
|
ZNF217
(details) |
13009 | zinc finger protein 217 | 7764 | O75362 | ZN217_HUMAN | zf-C2H2 PF00096 128-150 156-178 377-397 472-493 | # | # | # | # | ZNF | Zinc fingers, C2H2-type | Histone modification erase cofactor, TF | Histone acetylation, TF repressor | 12493763 | BHC, LSD-CoREST | DNA | # | # | 12493763 | A family of HDAC1,2-associated complexes includes proteins with a putative role in DNA binding such as ZNF261/XFIM (=ZMYM3), ZNF198/FIM (=ZMYM2), and ZNF217. | # |
|
ZNF711
(details) |
13128 | zinc finger protein 711 | 7552 | Q9Y462 | ZN711_HUMAN | Zfx_Zfy_act PF04704 62-356, zf-C2H2 PF00096 383-405 505-527 562-584 590-613 619-641 676-698 704-727 733-755 | Zfp711 | 3045342 | A2ANX9 | ZN711_MOUSE | ZNF | Zinc fingers, C2H2-type | Histone modification erase cofactor | Histone acetylation | 20346720 | # | histone | # | # | 20346720 | The PHD domain of PHF8 binds to H3K4me3 and colocalizes with H3K4me3 at transcription initiation sites. Furthermore, PHF8 interacts with another XMLR protein, ZNF711, which binds to a subset of PHF8 target genes, including the XLMR gene JARID1C. | # |
|
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. | # |