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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 cytokine | ||
| developmental process | ||
| dopamine metabolic process | ||
| exploration behavior | ||
| cellular response to cocaine |
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: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 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
Ortholog
| 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 |
