SMARCA4 and H3F3A

  • Number of citations of the paper that reports this interaction (PMID 15616580)
  • 80
  • Data Source:
  • HPRD (in vitro)

SMARCA4

H3F3A

Gene Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 H3 histone, family 3A
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 73 interactors: ACTB ACTL6A AHR AR ARID1A ARID1B ARID2 BRCA1 BRWD1 CARM1 CBX5 CCNE1 CDK19 CDK8 CDKN2A CDX2 CEBPA CEBPB CHD4 CHMP5 CIITA CREB1 CTNNB1 DPF3 ESR1 ETS2 FANCA GATA1 GMNN H2AFX H3F3A HIST1H3A HIST1H4F HIST2H2BE HIST2H3C HSF1 HSF4 IKZF1 KLF1 MBD3 MDM2 MED17 MED6 MKL1 MPHOSPH6 MPP6 MYC MYOCD NR3C1 NR4A2 PABPN1 PAX6 PBRM1 PHB RAP1A RB1 RBL1 RBL2 RELB RFXAP SIN3A SIN3B SMARCB1 SMARCC1 SMARCE1 SS18 SS18L1 STAT2 STAT3 STK11 TMF1 TP53 ZMYND11 25 interactors: ASF1A ASF1B BPTF BRD1 CABIN1 CARM1 CBX3 CHD1 CREBBP DAXX KAT2B KMT2A MAPK9 NOS3 PARP10 SETD7 SMARCA1 SMARCA4 SMARCA5 SS18 SSRP1 SUPT16H TLE2 UHRF1 ZMYND11
Entrez ID 6597 3020
HPRD ID 04459 03082
Ensembl ID ENSG00000127616 ENSG00000163041
Uniprot IDs A7E2E1 B3KNW7 P51532 Q9HBD4 B2R4P9 P84243
PDB IDs 2GRC 2H60 3UVD 2L43 3ASK 3ASL 3AV2 3JVK 3MUK 3MUL 3QL9 3QLA 3QLC 4GNE 4GNF 4GNG 4GU0 4GUR 4GUS 4GY5 4H9N 4H9O 4H9P 4H9Q 4H9R 4H9S 4HGA 4L58
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
36me3  atrx  code  combinatorial  commonest  daxx  g34r  g34v  gbms  global  h3k  h3k27me3  h3k36me3  h3k4me3  h3k9me3  highlights  hist1h3b  idh1  innovative  k27m  mark  marks  notably  opportunity  pediatric  polycomb  tailored  trimethylation  underlies 
Tagcloud (Difference) ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
36me3  atrx  code  combinatorial  commonest  daxx  g34r  g34v  gbms  global  h3k  h3k27me3  h3k36me3  h3k4me3  h3k9me3  highlights  hist1h3b  idh1  innovative  k27m  mark  marks  notably  opportunity  pediatric  polycomb  tailored  trimethylation  underlies 
Tagcloud (Intersection) ?