UniProt | Protein Name |
---|---|
A0A140VJL3 |
|
P00492 |
|
GO Term | Evidence Code | PMID |
---|---|---|
hypoxanthine salvage | ||
T cell mediated cytotoxicity | ||
purine ribonucleoside salvage | ||
adenine metabolic process | ||
striatum development |
GO Term | Evidence Code | PMID |
---|---|---|
hypoxanthine phosphoribosyltransferase activity | ||
magnesium ion binding | ||
protein binding | ||
guanine phosphoribosyltransferase activity | ||
nucleotide binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:10652 | Alzheimer's disease | |
DOID:10718 | giardiasis | |
DOID:1074 | kidney failure | |
DOID:1094 | attention deficit hyperactivity disorder | |
DOID:10952 | nephritis | |
DOID:10965 | spastic diplegia | |
DOID:10968 | spastic monoplegia | |
DOID:10969 | hemiplegia | |
DOID:10970 | spastic quadriplegic cerebral palsy | |
DOID:1107 | esophageal carcinoma |
HPO ID | HPO Term |
---|---|
HP:0002149 | Hyperuricemia |
HP:0002179 | Opisthotonus |
HP:0002342 | Intellectual disability, moderate |
HP:0002421 | Poor head control |
HP:0002827 | Hip dislocation |
HP:0003149 | Hyperuricosuria |
HP:0003259 | Elevated circulating creatinine concentration |
HP:0003593 | Infantile onset |
HP:0003621 | Juvenile onset |
HP:0004322 | Short stature |
Disease ID | Disease Name |
---|---|
ORPHA:510 |
|
ORPHA:79233 |
|
OMIM:300322 |
|
OMIM:300323 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
173323 | WB:WBGene00013690 | ||
103178054 | CALMI01690 | ||
102354389 | LATCH17467 | ||
406259 | ZFIN:ZDB-GENE-040426-1918 | DANRE07528 | |
100528167 | ICTPU33979 | ||
108268988 | ICTPU33597 | ||
115205547 | SALTR113142 | ||
101163340 | ORYLA01437 | ||
100703204 | ORENI47815 | ||
779138 | Xenbase:XB-GENE-6078713 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024