SLC6A19, solute carrier family 6 member 19

SLC6A19, solute carrier family 6 member 19

• This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) binds and interacts with the angiotensin-converting enzyme 2 (ACE2) which, among other functions, acts as a chaperone for membrane trafficking of SLC6A19. [provided by RefSeq, Jun 2020]

• Gene Synonyms (B0AT1, HND, sodium-dependent neutral amino acid transporter B(0)AT1, sodium-dependent amino acid transporter system B0, solute carrier family 6 (neurotransmitter transporter), member 19, solute carrier family 6 (neutral amino acid transporter), member 19, system B(0) neutral amino acid transporter AT1, system B0 neutral amino acid transporter,)
• NCBI Gene ID: 340024
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q695T7
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 6 member 19 interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.