FANCL and C17orf70

  • Number of citations of the paper that reports this interaction (PMID 17396147)
  • 52
  • Data Source:
  • HPRD (in vivo, two hybrid)

FANCL

C17orf70

Gene Name Fanconi anemia, complementation group L chromosome 17 open reading frame 70
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 24 interactors: ACVR1 BMPR1B C17orf70 CCDC36 CHCHD3 DOCK8 EIF4ENIF1 FANCB FANCD2 FANCI GGN GRN HES1 IKZF3 KIFC3 LZTS2 PCNA RBM45 RIMBP3 SSX2IP TFCP2 TGFBR1 UBE2T UBE2W 4 interactors: APP FANCB FANCL MDFI
Entrez ID 55120 80233
HPRD ID 06997 07982
Ensembl ID ENSG00000115392 ENSG00000185504
Uniprot IDs B5MC31 B5MCZ6 Q9NW38 A4ZI32 Q0VG06
PDB IDs 3ZQS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
2p16  2q24  4p15  agencies  assisting  epilepsies  epilepsy  ethnically  filtering  generalised  governmental  grouping  harbouring  heritability  ie  implicating  imputation  league  lumping  pcdh7  phenotyped  philanthropic  pleiotropically  protocadherin  scn1a  splitting  standardised  unclassified  vrk2 
Tagcloud (Difference) ?
2p16  2q24  4p15  agencies  assisting  epilepsies  epilepsy  ethnically  filtering  generalised  governmental  grouping  harbouring  heritability  ie  implicating  imputation  league  lumping  pcdh7  phenotyped  philanthropic  pleiotropically  protocadherin  scn1a  splitting  standardised  unclassified  vrk2 
Tagcloud (Intersection) ?