Gene: SLC1A4

Alternate names for this Gene: ASCT1|SATT|SPATCCM

Gene Summary: 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.

Gene is located in Chromosome: 2

Location in Chromosome : 2p14

Description of this Gene: solute carrier family 1 member 4

Type of Gene: protein-coding

Gene: LINC02245

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Gene: LOC107984063

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rs10194107 in SLC1A4;LINC02245;LOC107984063 gene and Serum albumin measurement PMID 22286219 2012 Genome-wide association study identifies multiple loci influencing human serum metabolite levels.