| Gene Symbol | DBH |
| Chromosome | 9q34.2 |
| Protein Type | Gene |
| Function | DBH catalyzes the oxidative hydroxylation of dopamine to produce norepinephrine. |
| Subcellular Localization | the Golgi apparatus and secretory vesicles of noradrenergic and adrenergic neurons. DBH deficiency |
| Molecular Weight | 73 kDa |
| Amino Acids | 603 aa |
| GeneCards | DBH |
| Human Protein Atlas | DBH |
| Gene | DBH (chromosome 9q34.2) |
| Protein Class | Copper-containing monooxygenase |
| Protein Size | 603 amino acids |
| Primary Localization | Golgi apparatus, secretory vesicles of noradrenergic neurons |
| Cofactor Requirement | Ascorbate (vitamin C), copper |
| Disease Associations | DBH deficiency, orthostatic hypotension, ADHD, schizophrenia, PD |
| Associated Diseases | ALS |
| Interactions | ADRA1A, ADRA2A, ADRB1, AMPK, APP, ATG5 |
| KG Connections | 61 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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