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:13417 | alexia | |
DOID:13487 | childhood disintegrative disease | |
DOID:13548 | secondary Parkinson disease | |
DOID:13593 | eclampsia | |
DOID:13620 | patent foramen ovale | |
DOID:13709 | premature ejaculation | |
DOID:13711 | dental fluorosis | |
DOID:13739 | nutmeg liver | |
DOID:1380 | endometrial cancer | |
DOID:13832 | patent ductus arteriosus |
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 |
---|---|---|---|
102028906 | CHILA11645 | ||
105718485 | AOTNA30553 | ||
110215186 | PHACI30652 | ||
101035559 | SAIBB37198 | ||
101961744 | ICTTR10660 | ||
101595207 | JACJA22844 | ||
102428822 | MYOLU12064 | ||
117017474 | RHIFE28381 | ||
100223814 | TAEGU05974 | ||
103222988 | CHLSB07121 |
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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