Title : Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

Pub. Date : 2015 Oct 15

PMID : 26206890






2 Functional Relationships(s)
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Compound Name
Protein Name
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1 The enzyme histamine N-methyltransferase (HNMT) inactivates HA by transferring a methyl group from S-adenosyl-l-methionine to HA, and is the only well-known pathway for termination of neurotransmission actions of HA in mammalian central nervous system. S-Adenosylmethionine histamine N-methyltransferase Homo sapiens
2 The enzyme histamine N-methyltransferase (HNMT) inactivates HA by transferring a methyl group from S-adenosyl-l-methionine to HA, and is the only well-known pathway for termination of neurotransmission actions of HA in mammalian central nervous system. S-Adenosylmethionine histamine N-methyltransferase Homo sapiens