MAOA
Sign in to saveAlso known as MAO-A, monoamine oxidase A, BRNRS
protein-coding gene in the species Homo sapiens
Gene data
MAOA- Name
- monoamine oxidase A
- Type
- protein-coding
- Chromosome
- X
- Position
- 43,654,907–43,746,821 (+)
- Aliases
- BRNRS, MAO-A
- Ensembl
- ENSG00000189221
- RefSeq RNA
- NM_000240.4, NM_001270458.2
- RefSeq protein
- NP_000231.1, NP_001257387.1
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 Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
monoamine oxidase A
- Symbol
- MAOA
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- Chr X:43,654,907-43,746,821
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Monoamine oxidase A 2BXS.png
Show 6 more facts
- HomoloGene ID
- 203
- Commons category
- Monoamine oxidase A
- exact match
- identifiers.org/ncbigene/4128
- genomic start
- 43515467
- genomic end
- 43746817
- cytogenetic location
- Xp11.3
Sources (9)
via Wikidata · CC0