UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to oxidative stress | ||
cellular response to phosphate starvation | ||
methylation | ||
visual learning | ||
response to wounding |
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:0060402 | chromosome 17p13.1 deletion syndrome | |
DOID:0060668 | anencephaly | |
DOID:0060776 | congenital diarrhea 5 with tufting enteropathy | |
DOID:0060877 | bullous congenital ichthyosiform erythroderma | |
DOID:0060888 | transient myeloproliferative syndrome | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060892 | late onset Parkinson's disease | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080016 | spina bifida |
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 |
---|---|---|---|
122138915 | CYPCA123985 | ||
103742059 | NANGA20735 | ||
116452864 | CORMO05899 | ||
103262083 | CARSF05188 | ||
115614190 | STRHB20046 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024