UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
renal albumin absorption | ||
norepinephrine secretion | ||
memory | ||
synaptic transmission, dopaminergic | ||
response to salt |
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:4464 | collecting duct carcinoma | |
DOID:4465 | papillary renal cell carcinoma | |
DOID:4467 | clear cell renal cell carcinoma | |
DOID:4471 | chromophobe renal cell carcinoma | |
DOID:4473 | sarcomatoid renal cell carcinoma | |
DOID:4480 | achondroplasia | |
DOID:4543 | retrograde amnesia | |
DOID:4621 | holoprosencephaly | |
DOID:4674 | androgen insensitivity syndrome | |
DOID:4676 | uremia |
HPO ID | HPO Term |
---|---|
HP:0002619 | Varicose veins |
HP:0002650 | Scoliosis |
HP:0002691 | Platybasia |
HP:0002721 | Immunodeficiency |
HP:0002901 | Hypocalcemia |
HP:0002960 | Autoimmunity |
HP:0002999 | Patellar dislocation |
HP:0003326 | Myalgia |
HP:0004322 | Short stature |
HP:0005435 | Impaired T cell function |
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