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:0050158 | desquamative interstitial pneumonia | |
DOID:0050328 | congenital hypothyroidism | |
DOID:0050427 | xeroderma pigmentosum | |
DOID:0050453 | lissencephaly | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050741 | alcohol dependence | |
DOID:0050742 | nicotine dependence | |
DOID:0050771 | pheochromocytoma | |
DOID:0050778 | Meckel syndrome | |
DOID:0050848 | obstructive sleep apnea |
HPO ID | HPO Term |
---|---|
HP:0000175 | Cleft palate |
HP:0000238 | Hydrocephalus |
HP:0000252 | Microcephaly |
HP:0000262 | Turricephaly |
HP:0000272 | Malar flattening |
HP:0000276 | Long face |
HP:0000286 | Epicanthus |
HP:0000316 | Hypertelorism |
HP:0000322 | Short philtrum |
HP:0000343 | Long philtrum |
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