Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13

J Intern Med. 1995 Sep;238(3):249-53. doi: 10.1111/j.1365-2796.1995.tb00931.x.

Abstract

Oncogenesis of tumours related to multiple endocrine neoplasia type 1 (MEN1) is associated with somatic deletions involving the MEN1 locus at chromosomal region 11q13, suggesting inactivation of a tumour-suppressor gene in this region. Here we describe the localization of the MEN1 gene to a 900-kb region, based on linkage analysis in affected families and deletion mapping of MEN1-associated tumours. In addition, a set of microsatellite markers mapped to the 11q11-13 region were used for linkage analysis in a large Tasmanian MEN1 pedigree, demonstrating the usefulness of these markers for presymptomatic testing in affected families.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 11 / genetics*
  • Genetic Linkage
  • Genotype
  • Heterozygote
  • Humans
  • Lod Score
  • Middle Aged
  • Multiple Endocrine Neoplasia Type 1 / genetics*
  • Pedigree
  • Tasmania