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:10825 | essential hypertension | |
DOID:1089 | tethered spinal cord syndrome | |
DOID:10892 | hypospadias | |
DOID:10907 | microcephaly | |
DOID:10908 | hydrocephalus | |
DOID:10914 | amnestic disorder | |
DOID:10915 | Wernicke-Korsakoff syndrome | |
DOID:10923 | sickle cell anemia | |
DOID:10930 | borderline personality disorder | |
DOID:10932 | obsessive-compulsive personality disorder |
HPO ID | HPO Term |
---|---|
HP:0001053 | Hypopigmented skin patches |
HP:0001061 | Acne |
HP:0001081 | Cholelithiasis |
HP:0001136 | Retinal arteriolar tortuosity |
HP:0001161 | Hand polydactyly |
HP:0001166 | Arachnodactyly |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
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