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:0060256 | Dowling-Degos disease | |
DOID:0060258 | reticulate acropigmentation of Kitamura | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060262 | gallbladder disease | |
DOID:0060306 | Meier-Gorlin syndrome | |
DOID:0060320 | inguinal hernia | |
DOID:0060321 | umbilical hernia | |
DOID:0060326 | myelomeningocele | |
DOID:0060327 | omphalocele |
HPO ID | HPO Term |
---|---|
HP:0000347 | Micrognathia |
HP:0000365 | Hearing impairment |
HP:0000369 | Low-set ears |
HP:0000385 | Small earlobe |
HP:0000389 | Chronic otitis media |
HP:0000396 | Overfolded helix |
HP:0000405 | Conductive hearing impairment |
HP:0000414 | Bulbous nose |
HP:0000426 | Prominent nasal bridge |
HP:0000431 | Wide nasal bridge |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115557386 | GADMO10047 | ||
101166546 | ORYLA14318 | ||
100693237 | ORENI58284 | ||
115582661 | SPAAU41170 | ||
379402 | Xenbase:XB-GENE-17337181 | ||
779254 | Xenbase:XB-GENE-6252788 | ||
108707135 | Xenbase:XB-GENE-6486206 | ||
549111 | Xenbase:XB-GENE-948947 | ||
549911 | Xenbase:XB-GENE-5865481 | ||
101942054 | CHRPI08201 |
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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