MAO-A Polyclonal Antibody, 50ul[BT-AP05200] Antibody Humanization Mutations in this gene cause

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

and a pseudogene of this gene is located on the long arm of chromosome 12

and belongs to the protein phosphatase 2C (PP2C) superfamily

Members of the serpin family generally complex with their target proteinases

The enzyme (dimethylglycine dehydrogenase) is found as a monomer in the mitochondrial matrix

MAO-A Polyclonal Antibody, 50ul[BT-AP05200] Antibody Humanization Mutations in this gene causeMAOA is one of two neighboring gene family members that encode Amine oxidase [flavin containing] A 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.