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SLC38A8


Official Full Name
solute carrier family 38 member 8
Organism
Homo sapiens
Gene ID
146167
Background
This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]
Synonyms
FVH2; FHASD; SNAT8

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