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: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 |
---|---|---|---|
100555105 | ANOCA11715 | ||
103670322 | URSMA16091 | ||
103672979 | URSMA26214 | ||
102544742 | VICPA01860 | ||
100950751 | OTOGA05955 | ||
105732276 | AOTNA36506 | ||
101053337 | SAIBB18644 | ||
101955334 | ICTTR01046 | ||
118319434 | SCOMX06085 | ||
102441052 | MYOLU00690 |
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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