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:585 | nephrolithiasis | |
DOID:6114 | cerebral convexity meningioma | |
DOID:615 | leukopenia | |
DOID:6193 | epithelioid sarcoma | |
DOID:633 | myositis | |
DOID:640 | encephalomyelitis | |
DOID:65 | connective tissue disease | |
DOID:653 | purine-pyrimidine metabolic disorder | |
DOID:6548 | angiomatous meningioma | |
DOID:655 | inherited metabolic disorder |
HPO ID | HPO Term |
---|---|
HP:0001347 | Hyperreflexia |
HP:0001419 | X-linked recessive inheritance |
HP:0001854 | Podagra |
HP:0001889 | Megaloblastic anemia |
HP:0001903 | Anemia |
HP:0001919 | Acute kidney injury |
HP:0001997 | Gout |
HP:0002013 | Vomiting |
HP:0002015 | Dysphagia |
HP:0002071 | Abnormality of extrapyramidal motor function |
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