FANCC and STMN2

  • Number of citations of the paper that reports this interaction (PubMedID 24676280)
  • 3
  • Data Source:
  • BioGRID (two hybrid, two hybrid)

FANCC

STMN2

Description FA complementation group C stathmin 2
Image No pdb structure No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Creutzfeldt-Jakob disease ( 19081515)
  • Frontotemporal dementia with GRN mutation (age at onset) ( 29724592)
  • Metabolite levels ( 23823483)
  • Response to serotonin reuptake inhibitors in major depressive disorder ( 25897834)
Interacting Genes 34 interacting genes: AZIN1 CAPN10 CCNA2 CDK1 CTBP1 DNAJB1 FANCA FANCD2 FANCE FANCF FANCG GSTP1 HSP90AA1 HSP90B1 HSPA1A HSPA4 HSPA8 IK KRT1 MEOX2 MT-ATP6 POR PRDX3 PRPF31 RPL18 RPS3A SPTA1 SPTAN1 STAT1 STMN1 STMN2 TCERG1 USP14 ZBTB32 19 interacting genes: CCDC85A CDK1 CEP70 EEF1A1 FANCC GPRASP1 GPRASP2 MAPK10 MAPK3 NGFR PRKACA PSMC1 RGS20 RGS6 TEX11 TFCP2 TRPC5 TXLNA UBE2I
Entrez ID 2176 11075
HPRD ID 01967 09003
Ensembl ID ENSG00000158169 ENSG00000104435
Uniprot IDs A0A024R9N2 A0A087WW44 B4E3W2 Q00597 Q93045
PDB IDs
Enriched GO Terms of Interacting Partners?
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