Gamma aminobutyric acid transaminase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A gamma-amino butyric acid metabolism disorder that is characterized by a defect in the gene coding for gamma-aminobutyrate transaminase, which is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. (Human Disease Ontology, DOID_0060174)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535407
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Genes

1 genes/proteins associated with the disease Gamma aminobutyric acid transaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ABAT 4-aminobutyrate aminotransferase 2.88009