UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to cytokine | ||
developmental process | ||
dopamine metabolic process | ||
exploration behavior | ||
cellular response to cocaine |
GO Term | Evidence Code | PMID |
---|---|---|
magnesium ion binding | ||
L-dopa O-methyltransferase activity |
|
|
orcinol O-methyltransferase activity |
|
|
protein binding | ||
catechol O-methyltransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050158 | desquamative interstitial pneumonia | |
DOID:0050328 | congenital hypothyroidism | |
DOID:0050427 | xeroderma pigmentosum | |
DOID:0050453 | lissencephaly | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050741 | alcohol dependence | |
DOID:0050742 | nicotine dependence | |
DOID:0050771 | pheochromocytoma | |
DOID:0050778 | Meckel syndrome | |
DOID:0050848 | obstructive sleep apnea |
HPO ID | HPO Term |
---|---|
HP:0002619 | Varicose veins |
HP:0002650 | Scoliosis |
HP:0002691 | Platybasia |
HP:0002721 | Immunodeficiency |
HP:0002901 | Hypocalcemia |
HP:0002960 | Autoimmunity |
HP:0002999 | Patellar dislocation |
HP:0003326 | Myalgia |
HP:0004322 | Short stature |
HP:0005435 | Impaired T cell function |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115557386 | GADMO10047 | ||
101166546 | ORYLA14318 | ||
100693237 | ORENI58284 | ||
115582661 | SPAAU41170 | ||
379402 | Xenbase:XB-GENE-17337181 | ||
779254 | Xenbase:XB-GENE-6252788 | ||
108707135 | Xenbase:XB-GENE-6486206 | ||
549111 | Xenbase:XB-GENE-948947 | ||
549911 | Xenbase:XB-GENE-5865481 | ||
101942054 | CHRPI08201 |
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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