UniProt | Protein Name |
---|---|
Q9VA73 |
|
A0A0B4KHW3 |
|
A0A0B4K6V1 |
|
GO Term | Evidence Code | PMID |
---|---|---|
L-aspartate transmembrane transport | ||
malate-aspartate shuttle | ||
wound healing | ||
L-glutamate transmembrane transport | ||
gluconeogenesis |
GO Term | Evidence Code | PMID |
---|---|---|
mitochondrial inner membrane | ||
mitochondrion |
GO Term | Evidence Code | PMID |
---|---|---|
calcium ion binding |
Gene Ontology |
---|
L-aspartate transmembrane transporter activity |
L-glutamate transmembrane transporter activity |
calcium ion binding |
malate-aspartate shuttle |
Location | References |
---|---|
DO ID | Disease Name | Source |
---|---|---|
DOID:0050432 | Asperger syndrome | |
DOID:0050696 | fetal alcohol spectrum disorder | |
DOID:0060041 | autism spectrum disorder | |
DOID:0070341 | neonatal-onset type II citrullinemia | |
DOID:0070342 | adult-onset type II citrullinemia | |
DOID:0080349 | developmental and epileptic encephalopathy 39 | |
DOID:12849 | autistic disorder | |
DOID:1852 | intrahepatic cholestasis | |
DOID:4137 | common bile duct disease | |
DOID:9273 | citrullinemia |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
8604 | HGNC:10982 | |||
10165 | HGNC:10983 | |||
50799 | MGI:1354721 | |||
78830 | MGI:1926080 | |||
175242 | WB:WBGene00019326 | |||
337675 | ZFIN:ZDB-GENE-031006-11 | |||
362145 | RGD:1305181 | |||
549674 | Xenbase:XB-GENE-1002100 | |||
856132 | SGD:S000006225 | |||
4800386 | 7237_1:000b19 |
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Last updated: December 9, 2024