SLC1A1 Chromosome 9

Solute carrier family 1 member 1
6 variants 6 Health Risk

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What This Gene Does
This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]
Gene Info
Gene Group
Solute carrier family 1
Locus Type
gene with protein product
Location
9p24.2
Ensembl
ENSG00000106688
Associated Conditions (3)
Dicarboxylic aminoaciduria
SLC1A1-related disorder
Cerebral visual impairment and intellectual disability
Key Variants
All Variants (6)
RSID Category Clinical Significance Conditions
RS142272329 Health Risk Conflicting classifications of pathogenicity Dicarboxylic aminoaciduria, Dicarboxylic aminoaciduria
RS143022823 Health Risk Conflicting classifications of pathogenicity Dicarboxylic aminoaciduria, SLC1A1-related disorder, Dicarboxylic aminoaciduria
RS144334183 Health Risk Conflicting classifications of pathogenicity Dicarboxylic aminoaciduria, Dicarboxylic aminoaciduria
RS147404292 Health Risk Conflicting classifications of pathogenicity Dicarboxylic aminoaciduria, Dicarboxylic aminoaciduria
RS147832850 Health Risk Conflicting classifications of pathogenicity Dicarboxylic aminoaciduria, Dicarboxylic aminoaciduria
RS755579388 Health Risk Likely pathogenic Cerebral visual impairment and intellectual disability, Cerebral visual impairment and intellectual disability
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