SMARCA4 and ARID2

  • Number of citations of the paper that reports this interaction (PMID 15985610)
  • 53
  • Data Source:
  • HPRD (in vivo)

SMARCA4

ARID2

Gene Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 AT rich interactive domain 2 (ARID, RFX-like)
Image No pdb structure
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 4 interactors: CCNA1 NFYC SMARCA4 SMARCE1
Entrez ID 6597 196528
HPRD ID 04459 16505
Ensembl ID ENSG00000127616 ENSG00000189079
Uniprot IDs A7E2E1 B3KNW7 P51532 Q9HBD4 Q68CP9
PDB IDs 2GRC 2H60 3UVD
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 
aberrations  applying  axin1  cdk15  cps1  creating  deleterious  disruptions  drive  driver  fn1  fusions  genomes  hccs  hnf4a  integrations  intronic  mll4  recurrently  rps6ka3  seq  silent  splice  tert  thrap3  transcriptomes  transcriptomic  tsc1  wgs 
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 
aberrations  applying  axin1  cdk15  cps1  creating  deleterious  disruptions  drive  driver  fn1  fusions  genomes  hccs  hnf4a  integrations  intronic  mll4  recurrently  rps6ka3  seq  silent  splice  tert  thrap3  transcriptomes  transcriptomic  tsc1  wgs 
Tagcloud (Intersection) ?