FANCA and SPTAN1

  • Number of citations of the paper that reports this interaction (PMID 10551855)
  • 15
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vivo)

FANCA

SPTAN1

Gene Name Fanconi anemia, complementation group A spectrin, alpha, non-erythrocytic 1
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 48 interactors: ABI1 ABL1 ACP1 ACTA1 ACTB ADD1 ANK1 CAPN1 CASP3 CASP7 CEP63 CTNNA1 DDX24 DES DISC1 EPB41 EPB41L2 EPB42 ERCC4 EVL EXOC1 FANCA FANCC GAP43 GRIA2 GRIN1 GRIN2A GRIN2B GRIN2D MAPK6 NEFL PIN4 PLEC PLEKHA5 PRKCB PTOV1 SHANK1 SHANK3 SLC9A2 SOS1 SPTB SPTBN1 SRC STAT1 SYN1 TANC1 TES TSSC4
Entrez ID 2175 6709
HPRD ID 06186 01684
Ensembl ID ENSG00000187741 ENSG00000197694
Uniprot IDs H3BSR5 O15360 Q86U55 Q13813
PDB IDs 2FOT 3F31 3FB2
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 
adenocarcinomas  atxn2  biology  consistently  couple  deregulation  dhx9  driver  exome  hundreds  kras  mutations  myof  never  overlap  preferentially  ptpn13  recurrent  respective  rps6kb2  seq  sequenced  smokers  somatic  sp1  stratification  targetable  ten  thousands 
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 
adenocarcinomas  atxn2  biology  consistently  couple  deregulation  dhx9  driver  exome  hundreds  kras  mutations  myof  never  overlap  preferentially  ptpn13  recurrent  respective  rps6kb2  seq  sequenced  smokers  somatic  sp1  stratification  targetable  ten  thousands 
Tagcloud (Intersection) ?