Skip Navigation Links Home » Resources » Gene Detail

ASMT, acetylserotonin O-methyltransferase

Matching ORF Clones

Request a Custom Clone

Don't see what you need?

Request My Custom Clone »
  • Gene Overview
  • Interaction Network
  • Sequence Verification

ASMT, acetylserotonin O-methyltransferase

  • This gene belongs to the methyltransferase superfamily, and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. The encoded enzyme catalyzes the final reaction in the synthesis of melatonin, and is abundant in the pineal gland. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2010]

  • Gene Synonyms (acetylserotonin O-methyltransferase, acetylserotonin N-methyltransferase, acetylserotonin methyltransferase (Y chromosome), hydroxyindole O-methyltransferase, ASMTY, HIOMT, HIOMTY,)
  • NCBI Gene ID: 438
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024RBT9
    UNIPROT ID#>>X5D784
    UNIPROT ID#>>P46597
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

acetylserotonin O-methyltransferase interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

It appears that you have Javascript disabled. Our website requires Javascript to function correctly. For the best browsing experience, please enable Javascript.