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MAOA
Anti-MAOA Recombinant Antibody Products
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For Research Use Only. Not For Clinical Use.
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]
Protein class
Disease related genes, Enzymes, FDA approved drug targets, Human disease related genes, Metabolic proteins
Predicted location
Membrane
Single cell type specificity
Cell type enhanced (Proximal enterocytes, Proximal tubular cells, Undifferentiated cells)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Cell line enhanced (ASC diff, HHSteC, HSkMC, hTCEpi, RT4)
Interaction
Monomer, homo- or heterodimer (containing two subunits of similar size). Each subunit contains a covalently bound flavin. Enzymatically active as monomer.
Molecular function
Oxidoreductase
More Types Infomation
Related Diseases
Amphetamine Addiction