FANCA and SMARCA4

  • Number of citations of the paper that reports this interaction (PMID 11726552)
  • 15
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (two hybrid, in vitro, in vivo)

FANCA

SMARCA4

Gene Name Fanconi anemia, complementation group A SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 46 interactors: AKT1 ALDOA ATP5B ATR AZIN1 BRCA1 CAPN1 CCT3 CD79A CDK1 CENPE DAXX DDX39B DNAJB1 DUS4L ENO1 FANCC FANCE FANCF FANCG GNB2 HES1 HPRT1 HSP90AA1 IFIT3 IKBKB KRT1 LIPG MKNK1 MX1 NAMPT NUB1 PRPF31 PSMA5 RPL18 SGK1 SMARCA4 SMARCC1 SMARCD3 SNX5 SPTAN1 TAF10 TCERG1 TCP1 TPT1 ZNF24 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 2175 6597
HPRD ID 06186 04459
Ensembl ID ENSG00000187741 ENSG00000127616
Uniprot IDs H3BSR5 O15360 Q86U55 A7E2E1 B3KNW7 P51532 Q9HBD4
PDB IDs 2GRC 2H60 3UVD
Enriched GO Terms of Interacting Partners?
Tagcloud ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
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) ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
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 (Intersection) ?