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: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:0002101 | Abnormal lung lobation |
HP:0002139 | Arrhinencephaly |
HP:0002239 | Gastrointestinal hemorrhage |
HP:0002251 | Aganglionic megacolon |
HP:0002353 | EEG abnormality |
HP:0002381 | Aphasia |
HP:0002414 | Spina bifida |
HP:0002435 | Meningocele |
HP:0002566 | Intestinal malrotation |
HP:0002607 | Bowel incontinence |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109312767 | CROPO18909 | ||
113446487 | PSETE19657 | ||
100545849 | MELGA04739 | ||
103818085 | SERCA12886 | ||
100934159 | SARHA07002 | ||
103123291 | ERIEU02845 | ||
712548 | MACMU00872 | ||
101022593 | PAPAN12086 | ||
458655 | PANTR25982 | ||
445450 | CANLF10595 |
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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