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:0001744 | Splenomegaly |
HP:0001762 | Talipes equinovarus |
HP:0001829 | Foot polydactyly |
HP:0001872 | Abnormality of thrombocytes |
HP:0001873 | Thrombocytopenia |
HP:0001999 | Abnormal facial shape |
HP:0002019 | Constipation |
HP:0002020 | Gastroesophageal reflux |
HP:0002023 | Anal atresia |
HP:0002099 | Asthma |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
104681986 | RHIRO39893 | ||
114586245 | PODMU27645 | ||
107553993 | SINGR08682 | ||
107584930 | SINGR34375 | ||
107601759 | SINGR65043 | ||
116819462 | CHEAB13616 | ||
115043895 | ECHNA05008 | ||
115388414 | SALFA35247 | ||
113485994 | ATHCN16216 | ||
109098298 | CYPCA119631 |
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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