GGN and FANCL

  • Number of citations of the paper that reports this interaction (PMID 12574169)
  • 10
  • Data Source:
  • HPRD (in vivo, two hybrid)

GGN

FANCL

Gene Name gametogenetin Fanconi anemia, complementation group L
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 7 interactors: BRCA1 ECT2 FANCL GGNBP1 GGNBP2 KRT40 OAZ3 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
Entrez ID 199720 55120
HPRD ID 17036 06997
Ensembl ID ENSG00000179168 ENSG00000115392
Uniprot IDs Q86UU5 B5MC31 B5MCZ6 Q9NW38
PDB IDs 3ZQS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
bcg  bovis  confocal  domain  except  gfp  gga  immunoblot  immunofluorescence  localization  localizes  maintain  missing  mtb  mycobacteria  mycobacterial  mycobacterium  pathogenic  pe  pgrs  pgrs30  polar  poles  repeats  repetitive  smegmatis  tagged  unique  virulence 
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) ?
bcg  bovis  confocal  domain  except  gfp  gga  immunoblot  immunofluorescence  localization  localizes  maintain  missing  mtb  mycobacteria  mycobacterial  mycobacterium  pathogenic  pe  pgrs  pgrs30  polar  poles  repeats  repetitive  smegmatis  tagged  unique  virulence 
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) ?