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:0000739 | Anxiety |
HP:0000746 | Delusion |
HP:0000765 | Abnormal thorax morphology |
HP:0000778 | Hypoplasia of the thymus |
HP:0000821 | Hypothyroidism |
HP:0000829 | Hypoparathyroidism |
HP:0000836 | Hyperthyroidism |
HP:0000929 | Abnormal skull morphology |
HP:0000979 | Purpura |
HP:0001051 | Seborrheic dermatitis |
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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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024