GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of aspartate secretion | ||
positive regulation of dopamine metabolic process | ||
response to xenobiotic stimulus | ||
cerebellum development | ||
behavioral response to cocaine |
GO Term | Evidence Code | PMID |
---|---|---|
4-aminobutyrate transaminase complex | ||
mitochondrial matrix |
|
|
mitochondrion |
GO Term | Evidence Code | PMID |
---|---|---|
4-aminobutyrate transaminase activity | ||
succinate-semialdehyde dehydrogenase binding | ||
4-aminobutyrate:2-oxoglutarate transaminase activity | ||
pyridoxal phosphate binding | ||
metal ion binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050561 | Lennox-Gastaut syndrome | |
DOID:0050562 | West syndrome | |
DOID:0050741 | alcohol dependence | |
DOID:0050908 | myelodysplastic syndrome | |
DOID:0060041 | autism spectrum disorder | |
DOID:0060174 | GABA aminotransferase deficiency | |
DOID:0060672 | Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | |
DOID:0080855 | Parkinsonism | |
DOID:0090103 | Huntington's disease-like 1 | |
DOID:0090104 | Huntington's disease-like 2 |
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 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
177897 | WB:WBGene00001794 | ||
40188 | FB:FBgn0036927 | ||
103178828 | CALMI16436 | ||
102355159 | LATCH04020 | ||
378968 | ZFIN:ZDB-GENE-031006-4 | DANRE30908 | |
113572841 | ELEEL12014 | ||
115171987 | SALTR93039 | ||
115208398 | SALTR26911 | ||
100698450 | ORENI55446 | ||
398751 | Xenbase:XB-GENE-957497 |
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: August 19, 2024