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:9505 | cannabis abuse | |
DOID:9521 | Laron syndrome | |
DOID:9588 | encephalitis | |
DOID:9719 | neovascular inflammatory vitreoretinopathy | |
DOID:9744 | type 1 diabetes mellitus | |
DOID:9854 | lingual-facial-buccal dyskinesia | |
DOID:9884 | muscular dystrophy | |
DOID:9923 | developmental coordination disorder | |
DOID:9952 | acute lymphoblastic leukemia | |
DOID:9953 | acute biphenotypic leukemia |
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 |
---|---|---|---|
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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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024