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:1389 | polyneuropathy | |
DOID:13918 | somatization disorder | |
DOID:13976 | peptic esophagitis | |
DOID:14159 | obstructive hydrocephalus | |
DOID:14221 | abdominal obesity-metabolic syndrome 1 | |
DOID:14250 | Down syndrome | |
DOID:14320 | generalized anxiety disorder | |
DOID:14330 | Parkinson's disease | |
DOID:14402 | critical illness polyneuropathy | |
DOID:1443 | cerebral degeneration |
HPO ID | HPO Term |
---|---|
HP:0000582 | Upslanted palpebral fissure |
HP:0000600 | Abnormality of the pharynx |
HP:0000627 | Posterior embryotoxon |
HP:0000648 | Optic atrophy |
HP:0000670 | Carious teeth |
HP:0000682 | Abnormal dental enamel morphology |
HP:0000708 | Atypical behavior |
HP:0000716 | Depression |
HP:0000717 | Autism |
HP:0000738 | Hallucinations |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102028906 | CHILA11645 | ||
105718485 | AOTNA30553 | ||
110215186 | PHACI30652 | ||
101035559 | SAIBB37198 | ||
101961744 | ICTTR10660 | ||
101595207 | JACJA22844 | ||
102428822 | MYOLU12064 | ||
117017474 | RHIFE28381 | ||
100223814 | TAEGU05974 | ||
103222988 | CHLSB07121 |
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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