FANCC and STMN2

  • 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 54 interacting genes: APC AZIN1 BMPR1A BUB1 CAPN10 CCNA2 CCND1 CDK1 CTBP1 DLC1 DNAJB1 EGFR FANCA FANCD2 FANCE FANCF FANCG FBXW7 GSTP1 HSP90AA1 HSP90B1 HSPA1A HSPA4 HSPA8 IK KRAS KRT1 MEOX2 MLH3 MT-ATP6 MUTYH NRAS PDGFRL PIK3CA PMS2 POR PRDX3 PRPF31 PTPN12 PTPRJ RB1 RPL18 RPS3A SMAD4 SPTA1 SPTAN1 SRC STAT1 STMN1 STMN2 TCERG1 TGFBR2 USP14 ZBTB32 28 interacting genes: CCDC85A CCHCR1 CDC42 CDK1 CEP70 CTNNA3 EEF1A1 ERBB2 FAM90A1 FANCC GPRASP1 GPRASP2 MAPK10 MAPK3 MBD3 NGFR NTAQ1 PRKACA PSMB1 PSMC1 RGS20 RGS6 SESTD1 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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