C17orf50 and VWC2L

		C17orf50	VWC2L
Description		chromosome 17 open reading frame 50	von Willebrand factor C domain containing 2 like
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		Blood protein levels ( 28240269) Cerebrospinal AB1-42 levels in normal cognition ( 29274321)	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		11 interacting genes: ANKS1A CIB3 CTNNA3 KRT34 KRTAP10-1 KRTAP10-5 KRTAP10-8 MGAT5B PCSK5 VWC2L ZNF587	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
Entrez ID		146853	402117
HPRD ID		11239	19160
Ensembl ID		ENSG00000270806	ENSG00000174453
Uniprot IDs		Q8WW18	B2RUY7 B7ZW27
PDB IDs
Enriched GO Terms of Interacting Partners?
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