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:5041 | esophageal cancer | |
DOID:5165 | uterine corpus sarcoma | |
DOID:5213 | chronic inflammatory demyelinating polyradiculoneuropathy | |
DOID:529 | blepharospasm | |
DOID:543 | dystonia | |
DOID:557 | kidney disease | |
DOID:5603 | T-cell acute lymphoblastic leukemia | |
DOID:5604 | adult acute lymphocytic leukemia | |
DOID:5672 | large intestine cancer | |
DOID:580 | uric acid nephrolithiasis |
HPO ID | HPO Term |
---|---|
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001263 | Global developmental delay |
HP:0001266 | Choreoathetosis |
HP:0001270 | Motor delay |
HP:0001332 | Dystonia |
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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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