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:0050865 | tongue squamous cell carcinoma | |
DOID:0060001 | withdrawal disorder | |
DOID:0060041 | autism spectrum disorder | |
DOID:0060058 | lymphoma | |
DOID:0060060 | non-Hodgkin lymphoma | |
DOID:0060165 | Kleine-Levin syndrome | |
DOID:0060167 | seasonal affective disorder | |
DOID:0060185 | Clostridium difficile colitis | |
DOID:0060215 | Balo concentric sclerosis | |
DOID:0060249 | scoliosis |
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 |
---|---|---|---|
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