NP_001119807.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
53,481 Da
NCBI Official Full Name
B(0,+)-type amino acid transporter 1
NCBI Official Synonym Full Names
solute carrier family 7 member 9
NCBI Official Synonym Symbols
NCBI Protein Information
B(0,+)-type amino acid transporter 1
UniProt Protein Name
b(0,+)-type amino acid transporter 1
UniProt Synonym Protein Names
Glycoprotein-associated amino acid transporter b0,+AT1; Solute carrier family 7 member 9
UniProt Synonym Gene Names
NCBI Summary for SLC7A9
This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011]
UniProt Comments for SLC7A9
Involved in the high-affinity, sodium-independent transport of cystine and neutral and dibasic amino acids (system b(0,+)-like activity). Thought to be responsible for the high-affinity reabsorption of cystine in the kidney tubule.
Research Articles on SLC7A9
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Pathways associated with SLC7A9 recombinant protein
Diseases associated with SLC7A9 recombinant protein
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