| MAOA |
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| Available structures |
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| PDB | Ortholog search: PDBe RCSB |
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| Identifiers |
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| Aliases | MAOA, MAO-A, monoamine oxidase A, BRNRS |
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| External IDs | OMIM: 309850; MGI: 96915; HomoloGene: 203; GeneCards: MAOA; OMA:MAOA - orthologs |
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| Gene location (Mouse) |
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| | Chr. | X chromosome (mouse)[2] |
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| | Band | X A1.2|X 11.78 cM | Start | 16,485,937 bp[2] |
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| End | 16,554,057 bp[2] |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - mucosa of ileum
- mucosa of colon
- mucosa of sigmoid colon
- right lung
- jejunal mucosa
- duodenum
- rectum
- parotid gland
- gastric mucosa
- mucosa of transverse colon
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| | Top expressed in | - left colon
- superior cervical ganglion
- jejunum
- duodenum
- intestinal villus
- Ileal epithelium
- stroma of bone marrow
- endothelial cell of lymphatic vessel
- crypt of lieberkuhn of small intestine
- Paneth cell
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| | More reference expression data |
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| BioGPS | |
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| Gene ontology |
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| Molecular function | | | Cellular component | | | Biological process | | | Sources:Amigo / QuickGO |
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| Wikidata |
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Monoamine oxidase A, also known as MAO-A, is an enzyme (E.C. 1.4.3.4) that in humans is encoded by the MAOA gene.[5][6] This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as norepinephrine, serotonin and tyramine. A mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed.[7]