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:0090053 | episodic kinesigenic dyskinesia 1 | |
DOID:0090054 | episodic kinesigenic dyskinesia 2 | |
DOID:0090103 | Huntington's disease-like 1 | |
DOID:0090104 | Huntington's disease-like 2 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 | |
DOID:0110038 | Alzheimer's disease 6 | |
DOID:0110039 | Alzheimer's disease 7 | |
DOID:0110041 | Alzheimer's disease 8 | |
DOID:0110043 | Alzheimer's disease 10 |
HPO ID | HPO Term |
---|---|
HP:0001263 | Global developmental delay |
HP:0001281 | Tetany |
HP:0001300 | Parkinsonism |
HP:0001328 | Specific learning disability |
HP:0001369 | Arthritis |
HP:0001382 | Joint hypermobility |
HP:0001508 | Failure to thrive |
HP:0001511 | Intrauterine growth retardation |
HP:0001513 | Obesity |
HP:0001537 | Umbilical hernia |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100770626 | CRIGR10028 | ||
12846 | MGI:88470 | MOUSE19552 | |
24267 | RGD:2379 | RATNO04095 | |
100730509 | CAVPO02949 | ||
101868760 | MELUD10030 | ||
103669258 | URSMA27549 | ||
114041134 | VOMUR28364 | ||
113907191 | BOBOX32740 | ||
100960126 | OTOGA01943 | ||
101070611 | TAKRU21784 |
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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