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SLC32A1

solute carrier family 32 member 1

HCNC Approved Symbol
SLC32A1 (HGNC:11018)
Genomic Coordinates
20:38,724,486 - 38,729,372 (20q11.23)
Synonyms
VGAT, bA122O1.1, VIAAT
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Developmental and epileptic encephalopathy 114
620774AD
Generalized epilepsy with febrile seizures plus, type 12
620755AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC32A1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results