KCNJ13

Description		potassium inwardly rectifying channel subfamily J member 13
Image		No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Integral Component Of Membrane
	Molecular Function	Inward Rectifier Potassium Channel Activity
	Biological Process	Potassium Ion Transport Regulation Of Ion Transmembrane Transport Potassium Ion Import Across Plasma Membrane
Pathways
Drugs
Diseases		Leber congenital amaurosis (LCR) Vitreoretinal degeneration, including: Stickler syndrome type I (STL1); Stickler syndrome type II (STL2); Snowflake vitreoretinal degeneration (SVD); Wagner syndrome 1 (WGN1); Knobloch syndrome (KNO); Enhanced S-cone syndrome (ESCS); Autosomal dominant vitreoretinochoroidopathy (ADVIRC)
GWAS		Anxiety and stress-related disorders ( 31116379) Autism spectrum disorder or schizophrenia ( 28540026) Coronary artery disease ( 29212778) Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) ( 28714975) Schizophrenia ( 25056061 29483656 23974872)
Novel Interacting Genes		2 novel interacting genes: COL6A3 SLC25A17
Interacting Genes
Entrez ID		3769
HPRD ID		04441
Ensembl ID		ENSG00000115474
Uniprot IDs		O60928
PDB IDs
Enriched GO Terms of Interacting Partners?
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