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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1982 Jul;34(4):623–629.

Two previously undetected variants of glutamic-pyruvic transaminase found by acidic polyacrylamide gel electrophoresis.

T McLellan
PMCID: PMC1685356  PMID: 7102676

Abstract

Two new electrophoretic variants of glutamic-pyruvic transaminase (GPT) have been found by polyacrylamide gel electrophoresis at acidic pH. They appeared to represent a single allele, GPT 2, by the standard method of starch gel electrophoresis. Studies in families show that they are inherited as codominant alleles at the GPT locus. Population frequencies are about the same as those of other rare GPT variants. Their behavior on gels is consistent with both of them having substitutions of histidines in place of uncharged amino acids.

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Selected References

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  1. Cartwright G. E., Edwards C. Q., Kravitz K., Skolnick M., Amos D. B., Johnson A., Buskjaer L. Hereditary hemochromatosis. Phenotypic expression of the disease. N Engl J Med. 1979 Jul 26;301(4):175–179. doi: 10.1056/NEJM197907263010402. [DOI] [PubMed] [Google Scholar]
  2. Chen S. H., Giblett E. R., Anderson J. E., Fossum B. L. Genetics of glutamic-pyruvic transaminase: its inheritance, common and rare variants, population distribution, and differences in catalytic activity. Ann Hum Genet. 1972 Apr;35(4):401–409. [PubMed] [Google Scholar]
  3. Chen S. H., Giblett E. R. Polymorphism of soluble glutamic-pyruvic transaminase: a new genetic marker in man. Science. 1971 Jul 9;173(3992):148–149. doi: 10.1126/science.173.3992.148. [DOI] [PubMed] [Google Scholar]
  4. Fisher R. A., Putt W., Harris H. The distribution of isoelectric points of human soluble proteins and in particular of the enzyme products of 88 human gene loci. Ann Hum Genet. 1977 May;40(4):371–384. doi: 10.1111/j.1469-1809.1977.tb02025.x. [DOI] [PubMed] [Google Scholar]
  5. GARDNER E. J., STEPHENS F. E. Breast cancer in one family group. Am J Hum Genet. 1950 Mar;2(1):30–40. [PMC free article] [PubMed] [Google Scholar]
  6. Harrison R. A. The detection of hexokinase, glucosephosphate isomerase and phosphoglucomutase activities in polyacrylamide gels after electrophoresis: a novel method using immobilized glucose 6-phosphate dehydrogenase. Anal Biochem. 1974 Oct;61(2):500–507. doi: 10.1016/0003-2697(74)90417-5. [DOI] [PubMed] [Google Scholar]
  7. Kravitz K., Skolnick M., Cannings C., Carmelli D., Baty B., Amos B., Johnson A., Mendell N., Edwards C., Cartwright G. Genetic linkage between hereditary hemochromatosis and HLA. Am J Hum Genet. 1979 Sep;31(5):601–619. [PMC free article] [PubMed] [Google Scholar]
  8. Kömpf J., Ritter H. Polymorphism of alanine aminotransferase (E.C.2.7.6.1): common and rare alleles. Hum Genet. 1979 Oct 2;51(3):287–292. doi: 10.1007/BF00283396. [DOI] [PubMed] [Google Scholar]
  9. Ramshaw J. A., Coyne J. A., Lewontin R. C. The sensitivity of gel electrophoresis as a detector of genetic variation. Genetics. 1979 Dec;93(4):1019–1037. doi: 10.1093/genetics/93.4.1019. [DOI] [PMC free article] [PubMed] [Google Scholar]

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