SLC17A8

Description		solute carrier family 17 member 8
Image		No pdb structure
GO Annotations	Cellular Component	Multivesicular Body Integral Component Of Membrane Integral Component Of Synaptic Vesicle Membrane Synaptic Vesicle Membrane Perikaryon Axon Terminus Excitatory Synapse Apical Dendrite Basal Dendrite Glial Limiting End-foot Pericellular Basket
	Molecular Function	L-glutamate Transmembrane Transporter Activity Neurotransmitter Transmembrane Transporter Activity Symporter Activity Transmembrane Transporter Activity
	Biological Process	Neural Retina Development Ion Transport Sodium Ion Transport Anion Transport Brain Development Sensory Perception Of Sound L-glutamate Transmembrane Transport Synaptic Transmission, Glutamatergic Regulation Of Synapse Structure Or Activity Cochlea Development Neurotransmitter Loading Into Synaptic Vesicle
Pathways		Organic anion transporters Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
Drugs
Diseases
GWAS		Low density lipoprotein cholesterol levels ( 32154731) Squamous cell carcinoma ( 23341777)
Interacting Genes		4 interacting genes: CYP4F2 DNAJC5 TMEM120B YIPF6
Entrez ID		246213
HPRD ID		10457
Ensembl ID		ENSG00000179520
Uniprot IDs		Q8NDX2
PDB IDs
Enriched GO Terms of Interacting Partners?
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