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:0060402 | chromosome 17p13.1 deletion syndrome | |
DOID:0060668 | anencephaly | |
DOID:0060776 | congenital diarrhea 5 with tufting enteropathy | |
DOID:0060877 | bullous congenital ichthyosiform erythroderma | |
DOID:0060888 | transient myeloproliferative syndrome | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060892 | late onset Parkinson's disease | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080016 | spina bifida |
HPO ID | HPO Term |
---|---|
HP:0000175 | Cleft palate |
HP:0000238 | Hydrocephalus |
HP:0000252 | Microcephaly |
HP:0000262 | Turricephaly |
HP:0000272 | Malar flattening |
HP:0000276 | Long face |
HP:0000286 | Epicanthus |
HP:0000316 | Hypertelorism |
HP:0000322 | Short philtrum |
HP:0000343 | Long philtrum |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
112907521 | VULVU33181 | ||
100473702 | AILME11410 | ||
101691541 | MUSPF17595 | ||
101097022 | FELCA28433 | ||
122204090 | PANLE00895 | ||
101315750 | TURTR08182 | ||
100155530 | PIGXX07450 | ||
102191825 | CAPHI31540 | ||
100354142 | RABIT16661 | ||
105997224 | DIPOR20540 |
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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