PRPF31 and FANCA

  • Number of citations of the paper that reports this interaction (PMID 14499622)
  • 5
  • Data Source:
  • BioGRID (two hybrid)

PRPF31

FANCA

Gene Name pre-mRNA processing factor 31 Fanconi anemia, complementation group A
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 55 interactors: AES C1QTNF1 CALCOCO2 CCDC136 CCDC57 CDCA7L CEP70 FANCA GNB2L1 GOLGA2 HNRNPH2 HNRNPK JAKMIP2 KCTD6 KHDRBS2 KHDRBS3 KRT15 KRT40 KRTAP10-1 KRTAP10-3 KRTAP10-8 KRTAP10-9 LDOC1 LURAP1 MID2 MIPOL1 MKRN3 MTUS2 NHP2L1 NOTCH2NL PDE4DIP PHC2 PHF5A PNMA1 PNMA2 PPIH PRICKLE1 PRPF3 PRPF4 PSTPIP1 RBM25 RBM4 RBMY1A1 RBMY1F SIAH1 SSX2IP STX11 TADA2A TFIP11 TMCC2 TP53BP2 TRIM27 TSGA10 ZNF250 ZNF587 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
Entrez ID 26121 2175
HPRD ID 05917 06186
Ensembl ID ENSG00000105618 ENSG00000187741
Uniprot IDs E7ESA8 F1T0A4 F1T0A5 Q8WWY3 H3BSR5 O15360 Q86U55
PDB IDs 2OZB 3SIU 3SIV
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ala78leufsx99  amplified  autosomal  chinese  exons  families  frequencies  harbor  heterozygous  hong  kong  missense  modify  nonpathogenic  phe262serfsx59  pigmentosa  pro347leu  prph2  retina  retinitis  rho  screen  screened  simplex  stranded  thirteen  truncating  woman 
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 
Tagcloud (Difference) ?
ala78leufsx99  amplified  chinese  exons  families  frequencies  harbor  heterozygous  hong  kong  missense  modify  nonpathogenic  phe262serfsx59  pigmentosa  pro347leu  prph2  retina  retinitis  rho  screen  screened  simplex  stranded  thirteen  truncating  woman 
aml  anemia  aplastic  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
Tagcloud (Intersection) ?
autosomal