Novel point mutation in exon 12 of the glucose-6- phosphate dehydrogenase gene: G6PD FLORES

J Clin Lab Anal. 2004;18(2):129-31. doi: 10.1002/jcla.20010.

Abstract

In Portugal there are a wide variety of G6PD deficiency associated mutations. In an individual from the island of Flores of the Azorean archipelago, we report a new mutation in the G6PD gene that gives rise to a "moderate rate of G6PD deficiency" (12.6% of the normal activity) according to WHO criteria. Direct sequencing revealed a C-->A point mutation at position 1387 with the consequent substitution of an Argine by Serine. We designated this new mutation as G6PD FLORES. The mutation is associated with haplotype I ( - - + + - - ), using six intragenic RFLPs. This information may also be seen as contributing to the clarification of the genetic makeup of the Azorean population, founder mutations, and/or gene flow.

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Substitution
  • Exons
  • Genetics, Population
  • Glucosephosphate Dehydrogenase / genetics*
  • Glucosephosphate Dehydrogenase Deficiency / enzymology
  • Glucosephosphate Dehydrogenase Deficiency / genetics
  • Haplotypes
  • Humans
  • Male
  • Point Mutation*
  • Polymorphism, Restriction Fragment Length
  • Portugal

Substances

  • Glucosephosphate Dehydrogenase