Gene
mao
- ID
- ZDB-GENE-040329-3
- Name
- monoamine oxidase
- Symbol
- mao Nomenclature History
- Previous Names
-
- wu:fb68b05
- wu:fo76d11
- wu:fq38g06
- Z-MAO (1)
- zgc:85761
- Type
- protein_coding_gene
- Location
- Chr: 9 Mapping Details/Browsers
- Description
- Enables primary amine oxidase activity. Involved in cellular biogenic amine catabolic process. Predicted to be located in mitochondrial outer membrane. Is expressed in brain; digestive system; gill; heart; and neurons. Human ortholog(s) of this gene implicated in Brunner Syndrome; alcohol use disorder; autism spectrum disorder; neurodegenerative disease (multiple); and panic disorder. Orthologous to several human genes including MAOB (monoamine oxidase B).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 25 figures from 14 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:85761 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- 8 figures from Baronio et al., 2021
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Brunner Syndrome | Alliance | Brunner syndrome | 300615 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Amine oxidase | FAD/NAD(P)-binding domain superfamily | Flavin amine oxidase | Flavin Monoamine Oxidase |
|---|---|---|---|---|---|
|
UniProtKB:Q6NSN2
|
522 |
Interactions and Pathways
No data available
Plasmids
No data available