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COMT gene

catechol-O-methyltransferase

Key facts

Official symbol
COMT
Full name
COMT
Chromosome
22
Map location
22q11.21
Organism
Homo sapiens
NCBI Gene ID
1312
Also known as
HEL-S-98n

Function summary

Catechol-O-methyltransferase catalyzes the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine. This O-methylation results in one of the major degradative pathways of the catecholamine transmitters. In addition to its role in the metabolism of endogenous substances, COMT is important in the metabolism of catechol drugs used in the treatment of hypertension, asthma, and Parkinson disease. COMT is found in two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). The differences between S-COMT and MB-COMT reside within the N-termini. Several transcript variants are formed through the use of alternative translation initiation sites and promoters. [provided by RefSeq, Sep 2008].

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Data source: NCBI Gene · alsesAI Gene Library