UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to corticosterone | ||
catecholamine catabolic process | ||
cerebellar cortex morphogenesis | ||
behavioral fear response | ||
response to hypoxia |
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:1389 | polyneuropathy | |
DOID:13918 | somatization disorder | |
DOID:13976 | peptic esophagitis | |
DOID:14159 | obstructive hydrocephalus | |
DOID:14221 | abdominal obesity-metabolic syndrome 1 | |
DOID:14250 | Down syndrome | |
DOID:14320 | generalized anxiety disorder | |
DOID:14330 | Parkinson's disease | |
DOID:14402 | critical illness polyneuropathy | |
DOID:1443 | cerebral degeneration |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000023 | Inguinal hernia |
HP:0000028 | Cryptorchidism |
HP:0000047 | Hypospadias |
HP:0000076 | Vesicoureteral reflux |
HP:0000089 | Renal hypoplasia |
HP:0000113 | Polycystic kidney dysplasia |
HP:0000130 | Abnormality of the uterus |
HP:0000160 | Narrow mouth |
HP:0000164 | Abnormality of the dentition |
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