ARID1B and SMARCA4

  • Number of citations of the paper that reports this interaction (PMID 12200431)
  • 32
  • Data Source:
  • HPRD (in vivo, in vitro, two hybrid)

ARID1B

SMARCA4

Gene Name AT rich interactive domain 1B (SWI1-like) SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 5 interactors: CUL2 HIST2H2BE SMAD9 SMARCA2 SMARCA4 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
Entrez ID 57492 6597
HPRD ID 10660 04459
Ensembl ID ENSG00000049618 ENSG00000127616
Uniprot IDs Q8NFD5 A7E2E1 B3KNW7 P51532 Q9HBD4
PDB IDs 2CXY 2EH9 2GRC 2H60 3UVD
Enriched GO Terms of Interacting Partners?
Tagcloud ?
arid2  baf  bcl11a  bcl11b  brd9  calu  catalogue  constructs  cosmic  deposited  driver  establishment  existed  hairpin  knocked  mswi  mutated  ones  pearson  psuper  ranking  reporters  shrna  slippage  smarca4  snf  sublines  swi  typing 
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 
Tagcloud (Difference) ?
arid2  baf  bcl11a  bcl11b  brd9  calu  catalogue  constructs  cosmic  deposited  driver  establishment  existed  hairpin  knocked  mswi  mutated  ones  pearson  psuper  ranking  reporters  shrna  slippage  sublines  typing 
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  subunits  trisomy  truncating 
Tagcloud (Intersection) ?
smarca4  snf  swi