SLC6A19

SLC6A19
Identifiers
Aliases	SLC6A19, B0AT1, HND, solute carrier family 6 member 19
External IDs	MGI: 1921588 HomoloGene: 52819 GeneCards: SLC6A19
Gene location (Human) Chr. Chromosome 5 (human) Band No data available Start 1,201,595 bp End 1,225,117 bp
Gene location (Mouse) Chr. Chromosome 13 (mouse) Band No data available Start 73,679,745 bp End 73,704,865 bp
Gene ontology Molecular function • neurotransmitter:sodium symporter activity • neutral amino acid transmembrane transporter activity • symporter activity • amino acid transmembrane transporter activity Cellular component • integral component of membrane • brush border membrane • plasma membrane • integral component of plasma membrane • extracellular exosome • membrane Biological process • neurotransmitter transport • amino acid transport • neutral amino acid transport • response to nutrient • transmembrane transport • amino acid transmembrane transport • transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	340024	74338
Ensembl	ENSG00000174358	ENSMUSG00000021565
UniProt	Q695T7	Q9D687
RefSeq (mRNA)	NM_001003841	NM_028878
RefSeq (protein)	NP_001003841	NP_083154
Location (UCSC)	Chr 5: 1.2 – 1.23 Mb	Chr 5: 73.68 – 73.7 Mb
PubMed search

340024

74338

ENSG00000174358

ENSMUSG00000021565

Q695T7

Q9D687

NM_001003841

NM_028878

NP_001003841

NP_083154

Solute carrier family 6 member 19 also known as the sodium-dependent neutral amino acid transporter B(0)AT1 or system B(0) neutral amino acid transporter AT1 is a protein that in humans is encoded by the SLC6A19 gene.

SLC6A19 is a system B(0) transporter that mediates epithelial resorption of neutral amino acids across the apical membrane in the kidney and intestine.

Mutations in the SLC6A19 gene cause Hartnup disease.

...
Wikipedia