SLC32A1 Chromosome 20

Solute carrier family 32 member 1
5 variants 5 Health Risk

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What This Gene Does
The protein encoded by this gene is an integral membrane protein involved in gamma-aminobutyric acid (GABA) and glycine uptake into synaptic vesicles. The encoded protein is a member of amino acid/polyamine transporter family II. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Solute carrier family 32
Locus Type
gene with protein product
Location
20q11.23
Ensembl
ENSG00000101438
Associated Conditions (5)
Intellectual disability
Seizure
Developmental and epileptic encephalopathy 114
Generalized epilepsy with febrile seizures plus
type 12
Key Variants
All Variants (5)
RSID Category Clinical Significance Conditions
RS2145649990 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Seizure, Developmental and epileptic encephalopathy 114
RS2145650130 Health Risk Likely pathogenic Intellectual disability, Seizure, Developmental and epileptic encephalopathy 114
RS2145650002 Health Risk Pathogenic Seizure, Intellectual disability, Developmental and epileptic encephalopathy 114
RS2084284179 Health Risk Pathogenic/Likely pathogenic Generalized epilepsy with febrile seizures plus, type 12, Generalized epilepsy with febrile seizures plus
RS2084286998 Health Risk Pathogenic/Likely pathogenic Generalized epilepsy with febrile seizures plus, type 12, Generalized epilepsy with febrile seizures plus
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