Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia

Hum Genet. 1992 Jan;88(3):347-8. doi: 10.1007/BF00197272.

Abstract

The entire coding sequence of a Japanese class 1 variant (G6PD Tokyo) was amplified by the polymerase chain reaction from genomic DNA. Nucleotide analysis by a direct sequencing technique revealed a unique nucleotide substitution (1246 G to A) in exon 10, which predicts a Glu to Lys substitution at the 416th amino acid. This is another member of a conspicuous mutation cluster surrounding the putative NADP-binding domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Hemolytic / genetics*
  • Base Sequence
  • DNA / genetics
  • Glucosephosphate Dehydrogenase / genetics*
  • Humans
  • Isoenzymes / genetics*
  • Molecular Sequence Data
  • Polymerase Chain Reaction

Substances

  • Isoenzymes
  • DNA
  • Glucosephosphate Dehydrogenase