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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
catechol-O-methyltransferase
Summary
- Gene Symbol
-
- COMT
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative initiation
- Catecholamine metabolism
- Cell membrane
- Cytoplasm
- Direct protein sequencing
- Lipid metabolism
- Magnesium
- Metal-binding
- Methyltransferase
- Neurotransmitter degradation
- Phosphoprotein
- Reference proteome
- S-adenosyl-L-methionine
- Schizophrenia
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P21964 |
|
| A0A140VJG8 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| response to oxidative stress | ||
| cellular response to phosphate starvation | ||
| methylation | ||
| visual learning | ||
| response to wounding |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
localization [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| magnesium ion binding | ||
| L-dopa O-methyltransferase activity |
|
|
| orcinol O-methyltransferase activity |
|
|
| protein binding | ||
| catechol O-methyltransferase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| 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 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001561 | Polyhydramnios |
| HP:0001601 | Laryngomalacia |
| HP:0001611 | Hypernasal speech |
| HP:0001629 | Ventricular septal defect |
| HP:0001631 | Atrial septal defect |
| HP:0001636 | Tetralogy of Fallot |
| HP:0001641 | Abnormal pulmonary valve morphology |
| HP:0001643 | Patent ductus arteriosus |
| HP:0001646 | Abnormal aortic valve morphology |
| HP:0001660 | Truncus arteriosus |
| Disease ID | Disease Name |
|---|---|
| OMIM:181500 |
|
| ORPHA:567 |
|
| OMIM:167870 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100770626 | CRIGR10028 | ||
| 12846 | MGI:88470 | MOUSE19552 | |
| 24267 | RGD:2379 | RATNO04095 | |
| 100730509 | CAVPO02949 | ||
| 101868760 | MELUD10030 | ||
| 103669258 | URSMA27549 | ||
| 114041134 | VOMUR28364 | ||
| 113907191 | BOBOX32740 | ||
| 100960126 | OTOGA01943 | ||
| 101070611 | TAKRU21784 |
