Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13

Science. 1994 Sep 30;265(5181):2088-90. doi: 10.1126/science.8091231.

Abstract

A small proportion of breast cancer, in particular those cases arising at a young age, is due to the inheritance of dominant susceptibility genes conferring a high risk of the disease. A genomic linkage search was performed with 15 high-risk breast cancer families that were unlinked to the BRCA1 locus on chromosome 17q21. This analysis localized a second breast cancer susceptibility locus, BRCA2, to a 6-centimorgan interval on chromosome 13q12-13. Preliminary evidence suggests that BRCA2 confers a high risk of breast cancer but, unlike BRCA1, does not confer a substantially elevated risk of ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Breast Neoplasms / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 13*
  • Female
  • Genes, Retinoblastoma
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Humans
  • Lod Score
  • Male
  • Ovarian Neoplasms / genetics
  • Pedigree
  • Phenotype

Substances

  • Genetic Markers