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- Table of Contents
Facts about b(0,+)-type amino acid transporter 1.
.
Human | |
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Gene Name: | SLC7A9 |
Uniprot: | P82251 |
Entrez: | 11136 |
Belongs to: |
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amino acid-polyamine-organocation (APC) superfamily |
b(0,+)AT; b(0+)AT; B(0+)-type amino acid transporter 1; BAT1; bo+ amino acid transporter; CSNU3; FLJ94301; Glycoprotein-associated amino acid transporter b0+AT1; SLC7A9; solute carrier family 7 (cationic amino acid transporter, y+ system), member 9; Solute carrier family 7 member 9
Mass (kDA):
53.481 kDA
Human | |
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Location: | 19q13.11 |
Sequence: | 19; NC_000019.10 (32830511..32870957, complement) |
Expressed in the brush border membrane in the kidney (at protein level). Kidney, small intestine, liver and placenta.
Apical cell membrane; Multi-pass membrane protein.
PMID: 10471498 by Feliubadalo L., et al. Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (b0,+AT) of rBAT.
PMID: 10588648 by Pfeiffer R., et al. Luminal heterodimeric amino acid transporter defective in cystinuria.