SLC6A19

Description		solute carrier family 6 member 19
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GO Annotations	Cellular Component	Plasma Membrane Integral Component Of Plasma Membrane Apical Plasma Membrane Brush Border Membrane Extracellular Exosome
	Molecular Function	Protein Binding Amino Acid Transmembrane Transporter Activity Neutral Amino Acid Transmembrane Transporter Activity Symporter Activity
	Biological Process	Amino Acid Transmembrane Transport Amino Acid Transport Response To Nutrient Neutral Amino Acid Transport Sodium Ion Transmembrane Transport
Pathways		Amino acid transport across the plasma membrane Na+/Cl- dependent neurotransmitter transporters Defective SLC6A19 causes Hartnup disorder (HND) Defective SLC6A19 causes Hartnup disorder (HND)
Drugs
Diseases		Hartnup disorder Iminoglycinuria
GWAS		Pancreatic cancer ( 25086665) Urinary metabolite levels in chronic kidney disease ( 31959995) Urinary metabolites ( 26352407) Urine 6-bromotryptophan levels in chronic kidney disease ( 32572055)
Interacting Genes		1 interacting genes: ACE2
Entrez ID		340024
HPRD ID		10596
Ensembl ID		ENSG00000174358
Uniprot IDs		Q695T7
PDB IDs		6M17 6M18 6M1D
Enriched GO Terms of Interacting Partners?
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