Abat - 4-aminobutyrate aminotransferase Gene
Also Known as Gabat; beta-AlaAT
Species: Rattus norvegicus
Summary
Enables 4-aminobutyrate transaminase activity. Involved in several processes, including gamma-aminobutyric acid biosynthetic process; positive regulation of inhibitory postsynaptic potential; and regulation of secretion. Located in mitochondrial matrix and neuron projection. Used to study several diseases, including Huntington's disease; epilepsy (multiple); heroin dependence; ischemia; and mental depression. Biomarker of Parkinsonism. Human ortholog(s) of this gene implicated in Alzheimer's disease; GABA aminotransferase deficiency; and Huntington's disease. Orthologous to human ABAT (4-aminobutyrate aminotransferase). [provided by Alliance of Genome Resources, Apr 2022]
Abat Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_031003.2 | NP_112265.1 | 4-aminobutyrate aminotransferase, mitochondrial |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables 4-aminobutyrate:2-oxoglutarate transaminase activity |
IDA
IDA: Inferred from direct assay
|
10447691 | RGD |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in mitochondrial matrix |
IDA
IDA: Inferred from direct assay
|
3132542 | RGD |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
4-aminobutyrate aminotransferase, mitochondrial |
|
|