4-aminobutyrate aminotransferase
| UniProt | Protein Name |
|---|---|
| P80404 |
|
| H3BNQ7 |
|
| X5D8S1 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| response to hypoxia |
|
|
| copulation |
|
|
| locomotory behavior |
|
|
| response to xenobiotic stimulus |
|
|
| GABA metabolic process |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrial matrix |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| pyridoxal phosphate binding |
|
|
| pyridoxal phosphate binding |
|
|
| pyridoxal phosphate binding |
|
|
| succinate-semialdehyde dehydrogenase binding |
|
|
| 4-aminobutyrate:2-oxoglutarate transaminase activity |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060174 | GABA aminotransferase deficiency | |
| DOID:12858 | Huntington's disease | |
| DOID:10652 | Alzheimer's disease |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000098 | Tall stature |
| HP:0000278 | Retrognathia |
| HP:0000494 | Downslanted palpebral fissures |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001254 | Lethargy |
| HP:0001263 | Global developmental delay |
| HP:0001274 | Agenesis of corpus callosum |
| HP:0001321 | Cerebellar hypoplasia |
| Disease ID | Disease Name |
|---|---|
| OMIM:613163 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026