UniProt | Protein Name |
---|---|
A0A140VJL3 |
|
P00492 |
|
GO Term | Evidence Code | PMID |
---|---|---|
dopaminergic neuron differentiation | ||
hypoxanthine metabolic process | ||
positive regulation of dopamine metabolic process | ||
IMP metabolic process | ||
response to amphetamine |
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:0110849 | xeroderma pigmentosum group G | |
DOID:0110850 | xeroderma pigmentosum group B | |
DOID:0111095 | Fanconi anemia complementation group A | |
DOID:0112127 | HRPT-related hyperuricemia | |
DOID:10041 | dysplastic nevus syndrome | |
DOID:10223 | dermatomyositis | |
DOID:10283 | prostate cancer | |
DOID:10286 | prostate carcinoma | |
DOID:1056 | oculocerebrorenal syndrome | |
DOID:1059 | intellectual disability |
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 |
---|---|---|---|
108700178 | Xenbase:XB-GENE-17330668 | ||
394936 | Xenbase:XB-GENE-1014679 | ||
109310997 | CROPO18605 | ||
113446755 | PSETE20102 | ||
100548399 | MELGA12936 | ||
103824492 | SERCA22104 | ||
791108 | ORNAN23438 | ||
100406827 | CALJA47571 | ||
105586233 | CERAT20119 | ||
709186 | MACMU47279 |
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Last updated: August 19, 2024