VWC2L and CRCT1

  • Data Source:
  • BioGRID (two hybrid)

VWC2L

CRCT1

Description von Willebrand factor C domain containing 2 like cysteine rich C-terminal 1
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 27 interacting genes: 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 55 interacting genes: AGTRAP ALPP APLP1 CEP126 CHD3 CYP21A2 CYSRT1 EEF1A1 GRN IGSF21 KRTAP1-3 KRTAP10-1 KRTAP10-7 KRTAP10-8 KRTAP10-9 KRTAP12-3 KRTAP4-1 KRTAP4-11 KRTAP4-12 KRTAP4-2 KRTAP4-4 KRTAP4-5 KRTAP5-11 KRTAP5-2 KRTAP5-3 KRTAP5-4 KRTAP5-6 KRTAP5-7 KRTAP5-8 KRTAP5-9 KRTAP9-2 KRTAP9-3 LCE1C LCE1F LCE2B LCE2C LCE4A LRIF1 MACO1 MEOX2 NOTCH2NLA NUP62 OIT3 PLSCR4 PTN RGS17 RGS20 SDCBP2 SLC39A7 TGM1 TLE1 TRIM55 TRIM63 VIM VWC2L
Entrez ID 402117 54544
HPRD ID 19160 16635
Ensembl ID ENSG00000174453 ENSG00000169509
Uniprot IDs B2RUY7 B7ZW27 Q9UGL9
PDB IDs
Enriched GO Terms of Interacting Partners?
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