Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene

Am J Hum Genet. 1989 Jul;45(1):123-7.

Abstract

To define the molecular basis for the TaqI site alteration in the ornithine transcarbamylase (OTC) (E.C.2.1.3.3) gene of a female patient with mild OTC deficiency, we used a combination of genomic amplification followed by direct sequencing and oligodeoxyribonucleotide hybridization. We obtained evidence for a C-to-T substitution in exon 5 (codon 141) of this gene. This mutation generates a stop codon, in place of Arg, at amino acid 109 of the mature OTC protein. The mutation arose, de novo, in a germ cell of one of the parents.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Base Sequence
  • Blotting, Southern
  • Cytosine*
  • Exons*
  • Female
  • Genes*
  • Guanine*
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Nucleic Acid Hybridization
  • Ornithine Carbamoyltransferase / genetics
  • Ornithine Carbamoyltransferase Deficiency Disease*
  • Pedigree

Substances

  • Guanine
  • Cytosine
  • Ornithine Carbamoyltransferase