UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
renin secretion into blood stream | ||
response to inorganic substance | ||
artery development | ||
prostaglandin metabolic process | ||
multicellular organism growth |
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:11612 | polycystic ovary syndrome | |
DOID:11634 | myxedema | |
DOID:117 | heart cancer | |
DOID:11716 | prediabetes syndrome | |
DOID:11720 | distal myopathy | |
DOID:11755 | choledocholithiasis | |
DOID:11832 | visual epilepsy | |
DOID:11836 | clubfoot | |
DOID:11847 | coronary thrombosis | |
DOID:11870 | Pick's disease |
HPO ID | HPO Term |
---|---|
HP:0001263 | Global developmental delay |
HP:0001281 | Tetany |
HP:0001300 | Parkinsonism |
HP:0001328 | Specific learning disability |
HP:0001369 | Arthritis |
HP:0001382 | Joint hypermobility |
HP:0001508 | Failure to thrive |
HP:0001511 | Intrauterine growth retardation |
HP:0001513 | Obesity |
HP:0001537 | Umbilical hernia |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103183994 | CALMI28692 | ||
102363275 | LATCH17564 | ||
561372 | ZFIN:ZDB-GENE-050913-117 | DANRE42593 | |
565370 | ZFIN:ZDB-GENE-040724-164 | DANRE01869 | |
103025058 | ASTMX04013 | ||
108265311 | ICTPU30273 | ||
124625982 | ICTPU30274 | ||
113573090 | ELEEL08877 | ||
115150851 | SALTR33931 | ||
115168561 | SALTR76287 |
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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