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:0110111 | atrial heart septal defect 6 | |
DOID:0110112 | atrial heart septal defect 7 | |
DOID:0110113 | atrial heart septal defect 8 | |
DOID:0110114 | atrial heart septal defect 9 | |
DOID:0110213 | isolated cleft palate | |
DOID:0110629 | Wolfram syndrome 1 | |
DOID:0110843 | xeroderma pigmentosum group A | |
DOID:0110844 | xeroderma pigmentosum group C | |
DOID:0110845 | xeroderma pigmentosum group D | |
DOID:0110846 | xeroderma pigmentosum group E |
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 |
---|---|---|---|
109312767 | CROPO18909 | ||
113446487 | PSETE19657 | ||
100545849 | MELGA04739 | ||
103818085 | SERCA12886 | ||
100934159 | SARHA07002 | ||
103123291 | ERIEU02845 | ||
712548 | MACMU00872 | ||
101022593 | PAPAN12086 | ||
458655 | PANTR25982 | ||
445450 | CANLF10595 |
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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