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SLC1A4

Official Full Name
solute carrier family 1 member 4
Organism
Homo sapiens
GeneID
6509
Background
The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]
Synonyms
SATT; ASCT1; SPATCCM;

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