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Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8.

We report here a new mouse mutation, kat, that causes pleiotropic effects including facial dysmorphism, dwarfing, male sterility, anemia, and progressive polycystic kidney disease. kat (kidney anemia and testis) and a second allele, kat2J, that occurred on C57BL/ 6J were mapped to mouse chromosome (Chr) 8 using intra- and intersubspecific intercrosses. A high-resolution map for kat2J on Chr 8 was constructed using the F2 progeny from a cross between C57BL/6J-kat2J/+ and an inbred strain of Mus musculus castaneus (CAST/Ei). The kat2J mutation was localized between D8Mit129 and D8Mit128 with the gene order centromere-D8Mit100-(1.2 +/- 0.26 cM)-D8Mit231-(0.17 +/- 0.09 cM)-D8Mit129-(0.28 +/- 0.12 cM)-D8Mit128-(0.98 +/- 0.23 cM)-D8Mit25/D8Mit8. This segment is homologous to human Chr 19p. The two mutations at this locus that have occurred at The Jackson Laboratory will be invaluable for positional cloning and subsequent functional analysis of the mutated gene.

Pubmed ID: 9070925

Authors

  • Janaswami PM
  • Birkenmeier EH
  • Cook SA
  • Rowe LB
  • Bronson RT
  • Davisson MT

Journal

Genomics

Publication Data

February 15, 1997

Associated Grants

  • Agency: NIDDK NIH HHS, Id: DK49634
  • Agency: NIGMS NIH HHS, Id: GM46697
  • Agency: NCRR NIH HHS, Id: P40 RR01183

Mesh Terms

  • Animals
  • Chromosome Mapping
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Phenotype
  • Polycystic Kidney Diseases