VWC2L and C22orf39

  • Number of citations of the paper that reports this interaction (PubMedID 32296183)
  • 86
  • Data Source:
  • BioGRID (two hybrid)

VWC2L

C22orf39

Description von Willebrand factor C domain containing 2 like chromosome 22 open reading frame 39
Image No pdb structure No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) ( 31835028)
  • Degraded stimulus continuous performance test score ( 31596458)
  • Dietary fat liking ( 32516399)
  • Household income (MTAG) ( 31844048)
  • Neuroticism ( 29255261)
  • PR interval ( 23534349)
Interacting Genes 28 interacting genes: ATIC C17orf50 C22orf39 CEMP1 CRCT1 CXCL5 CYSRT1 DEFB112 FBXO34 FHL3 HOXA1 KRTAP10-8 KRTAP11-1 KRTAP19-2 LCE1A LCE1C LCE3A LCE5A MEOX2 NR4A3 OTX1 PPARA RIPK4 SPATA3 TRIM42 TYRO3 YPEL3 ZNF20 42 interacting genes: ANKS1A BANP CABP2 CEP76 COL8A1 CRYBA2 CYSRT1 DTX2 EXOSC8 FRS3 GNE GRN HSD3B7 ID2 ID3 INCA1 KRTAP10-1 KRTAP10-11 KRTAP10-3 KRTAP10-8 KRTAP10-9 KRTAP12-3 KRTAP13-2 KRTAP9-2 MAGEA11 MAPK8IP2 MDFI MGAT5B NFATC2IP PCSK5 PFDN5 PLSCR3 PPP2CB PSMA1 RBPMS RECK RIMBP3C SNX32 SYCE1L TRIB3 VWC2L ZNF620
Entrez ID 402117 128977
HPRD ID 19160 14041
Ensembl ID ENSG00000174453 ENSG00000242259
Uniprot IDs B2RUY7 B7ZW27 Q6P5X5
PDB IDs
Enriched GO Terms of Interacting Partners?
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