monoamine oxidase A
This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. 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. [provided by RefSeq, Jul 2012]
Gene aliases
MAO-A
Chromosome
X
Map location
Xp11.3
Gene type
protein-coding
Gene Ontology (GO) terms enrichment
Database references
Statistics for MAOA
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| Sequence variants | |
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| Protein-Protein Interactions |
Sequence variants for MAOA
List of cell lines/tissues that have MAOA sequence variants
List of pathways where MAOA is involved
| Pathway name | Pathway source |
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Protein-Protein Interaction Network for MAOA
Network key
Number of sequence variations per gene
Protein identification for MAOA
Browse by protein identification methods
| Identification method | Quantitative data available |
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