VWC2L and C17orf50

		VWC2L	C17orf50
Description		von Willebrand factor C domain containing 2 like	chromosome 17 open reading frame 50
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Extracellular Space AMPA Glutamate Receptor Complex Synapse
	Molecular Function	Protein Binding	Protein Binding
	Biological Process	Multicellular Organism Development Negative Regulation Of BMP Signaling Pathway Positive Regulation Of Neuron Differentiation
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)	Blood protein levels ( 28240269) Cerebrospinal AB1-42 levels in normal cognition ( 29274321)
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	11 interacting genes: ANKS1A CIB3 CTNNA3 KRT34 KRTAP10-1 KRTAP10-5 KRTAP10-8 MGAT5B PCSK5 VWC2L ZNF587
Entrez ID		402117	146853
HPRD ID		19160	11239
Ensembl ID		ENSG00000174453	ENSG00000270806
Uniprot IDs		B2RUY7 B7ZW27	Q8WW18
PDB IDs
Enriched GO Terms of Interacting Partners?
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