Chromosomal localization of a new mouse lens opacity gene (lop18)

Genomics. 1996 Aug 15;36(1):171-3. doi: 10.1006/geno.1996.0439.

Abstract

Examination of mouse strains with a slit lamp and indirect ophthalmoscopy revealed that strain CBA/CaGnLe has a white cataract obvious at weaning age. It soon progresses to a large white nuclear cataract with mild cortical changes. Crosses with C57BL/6J showed that this is inherited as a single recessive fully penetrant gene, which we have designated lop18 (lens opacity 18). Linkage analysis using visible marker T (brachyury), histocompatibility marker H2, and microsatellite markers D17Mit21, D17Mit28, D17Mit38, and D17Mit46 shows that the lop18 gene is located, approximately 16 cM from the centromere on mouse Chromosome 17. It is a likely candidate mutation for the alpha-crystallin (Crya1) gene.

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

  • Animals
  • Cataract / genetics*
  • Cataract / pathology
  • Chromosome Mapping*
  • Crosses, Genetic
  • Crystallins / genetics
  • Female
  • Genes, Recessive / genetics*
  • H-2 Antigens / genetics
  • Lens, Crystalline / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA

Substances

  • Crystallins
  • H-2 Antigens