Entity Details

Primary name MAOA
Entity type gene
Source Source Link

Details

PrimaryID4128
RefseqGeneNG_008957
SymbolMAOA
Namemonoamine oxidase A
ChromosomeX
LocationXp11.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1988-04-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsAOFA_HUMAN

GO terms

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GOName
GO:0005739 mitochondrion
GO:0005741 mitochondrial outer membrane
GO:0005829 cytosol
GO:0006576 cellular biogenic amine metabolic process
GO:0006805 xenobiotic metabolic process
GO:0008131 primary amine oxidase activity
GO:0009967 positive regulation of signal transduction
GO:0016021 integral component of membrane
GO:0019221 cytokine-mediated signaling pathway
GO:0042133 neurotransmitter metabolic process
GO:0042135 neurotransmitter catabolic process
GO:0042420 dopamine catabolic process
GO:0097621 monoamine oxidase activity

Diseases

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Disease IDSourceNameDescription
300615 OMIMBrunner syndrome (BRNRS)A form of X-linked non-dysmorphic mild mental retardation. Male patients are affected by borderline mental retardation and exhibit abnormal behavior, including disturbed regulation of impulsive aggression. Obligate female carriers have normal intelligence and behavior. The disease is caused by variants affecting the gene represented in this entry.

Interactions

13 interactions