Polymorphism of red cell glyoxalase I (EI: 4.4.1.5); a new genetic marker in man. Investigation of 169 mother-child combinations

Humangenetik. 1975;27(2):141-3. doi: 10.1007/BF00273329.

Abstract

The polymorphism of glyoxalase I was investigated in 169 mother-child combinations from southwestern Germany. Glyoxalase I (GLO) has 3 common phenotypes: GLO 1, GLO 2-1, and GLO 2. The results are in good agreement with the formal hypothesis: Two alleles GLO1 and GLO2 at an autosomal locus. The GLO1 gene frequency was estimated to be 0.39. From the electrophoretic pattern the GLO-molecule appears to consist of two subunits.

MeSH terms

  • Erythrocytes / enzymology*
  • Female
  • Gene Frequency
  • Germany, West
  • Glutathione
  • Glyoxal
  • Humans
  • Lyases*
  • Molecular Biology
  • Polymorphism, Genetic*

Substances

  • Glyoxal
  • Lyases
  • Glutathione