Genetic polymorphisms of glycine N-acyltransferase in Japanese individuals

Drug Metab Pharmacokinet. 2009;24(1):114-7. doi: 10.2133/dmpk.24.114.

Abstract

In the present study, we identified 5 novel single nucleotide polymorphisms (SNPs) in the gene ofglycine N-acyltransferase (GlyAT) by resequencing the entire coding region and the exon-intron junctions from 95 Japanese individuals. The allelic frequencies of 5 novel SNPs were 0.016 for -695T>C, 0.021 for -260C>T, 0.005 for 290C>T, 0.005 for 19371G>A, and 0.005 for 21289G>A. Genetic variants of -979C>G and 21409A>G were in perfect linkage disequilibrium with 21364A>G and 21422C>T, respectively. The nonsynonymous SNP, 21289G>A (Arg131His) in exon 5, was also genotyped in 31 Caucasian individuals, but none of them possessed 21289A (131His) allele.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases / genetics*
  • Asian People / genetics*
  • Base Sequence
  • DNA / genetics
  • Female
  • Gene Frequency
  • Humans
  • Inactivation, Metabolic / genetics
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Pharmaceutical Preparations / metabolism
  • Polymorphism, Single Nucleotide*

Substances

  • Pharmaceutical Preparations
  • DNA
  • Acyltransferases
  • glycine acyltransferase