SLC38A5
SLC38A5
Protein-coding gene in the species Homo sapiens
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene. [5]
SLC38A5 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | SLC38A5, JM24, SN2, SNAT5, pp7194, solute carrier family 38 member 5 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 300649 MGI: 2148066 HomoloGene: 24917 GeneCards: SLC38A5 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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The protein encoded by this gene is a system N sodium-coupled amino acid transporter. The encoded protein transports glutamine, asparagine, histidine, serine, alanine, and glycine across the cell membrane, but does not transport charged amino acids, imino acids, or N-alkylated amino acids. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined.
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: Solute carrier family 38 member 5". Retrieved 2017-10-07.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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