SLC17A5

Description		solute carrier family 17 member 5
Image		No pdb structure
GO Annotations	Cellular Component	Lysosome Lysosomal Membrane Cytosol Plasma Membrane Integral Component Of Plasma Membrane Membrane Integral Component Of Membrane Synaptic Vesicle Membrane
	Molecular Function	Carbohydrate:proton Symporter Activity Sialic Acid Transmembrane Transporter Activity Sialic Acid:proton Symporter Activity Transmembrane Transporter Activity
	Biological Process	Ion Transport Anion Transport Amino Acid Transport Response To Bacterium Sialic Acid Transport Carbohydrate Transmembrane Transport Proton Transmembrane Transport
Pathways		Sialic acid metabolism Organic anion transporters Defective SLC17A5 causes Salla disease (SD) and ISSD
Drugs
Diseases		Sialuria/ Sialic acid storage disease, including: Infantile sialic acid storage disease (ISSD); Sialuria, Finnish type / Salla disease (SD); Sialuria, French type
GWAS		Refractive error ( 32231278)
Interacting Genes		1 interacting genes: APP
Entrez ID		26503
HPRD ID		05058
Ensembl ID		ENSG00000119899
Uniprot IDs		Q9NRA2
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?