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SLC3A1

Official Full Name
solute carrier family 3 member 1
Organism
Homo sapiens
GeneID
6519
Background
This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Synonyms
D2H; ATR1; NBAT; RBAT; CSNU1;

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