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: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: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 |
---|---|---|---|
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