UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to oxidative stress | ||
cellular response to phosphate starvation | ||
methylation | ||
visual learning | ||
response to wounding |
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:0001053 | Hypopigmented skin patches |
HP:0001061 | Acne |
HP:0001081 | Cholelithiasis |
HP:0001136 | Retinal arteriolar tortuosity |
HP:0001161 | Hand polydactyly |
HP:0001166 | Arachnodactyly |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
104681986 | RHIRO39893 | ||
114586245 | PODMU27645 | ||
107553993 | SINGR08682 | ||
107584930 | SINGR34375 | ||
107601759 | SINGR65043 | ||
116819462 | CHEAB13616 | ||
115043895 | ECHNA05008 | ||
115388414 | SALFA35247 | ||
113485994 | ATHCN16216 | ||
109098298 | CYPCA119631 |
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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