Mapping Data

Experiment

• Experiment
  TEXT-QTL
• Chromosome
  5
• Reference
  J:82609 Haston CK, et al., Loci of intestinal distress in cystic fibrosis knockout mice. Physiol Genomics. 2003 Jan 15;12(2):79-84
• ID
  MGI:2670620

Genes

Gene	Assay Type
Cfsw2	visible phenotype
D5Mit239	PCR amplified length variant

Notes

• Experiment
  Genome scan of 156 loci was performed on a population of (B6.129P2-Cftr^tm1Unc x BALB/cJ-Cftr^tm1Unc)F2 animals to identify cystic fibrosis (CF) modifying QTLs. Males of parental strain BALB/cJ-Cftr^tm1Unc exhibit increased post-weaning survival compared to males of parental strain B6.129P2-Cftr^tm1Unc. Female animals from either strain do not exhibit this survival difference.
  
  A locus spanning a 25 cM interval on mouse Chromosome 10, Cfid, was identified in association with post-weaning survival andintestinal distress in male animals. Cfid exhibits peak linkage at D10Mit194 (29 cM) with P=1.2 x 10-4. BALB/cJ-derived alleles confer increased lethality and intestinal blockage at Cfid whereas C57BL/6J-derived alleles confer increased survival.
  
  Loci associated with survival to weaning were identified on mouse Chromosomes 3, 5, and X. Cfsw1 mapped to 49.7 cM on mouse Chromosome 3 and is associated with survival to weaning in female animals. Cfsw1 exhibits peak linkage at D3Mit189 (P=1.7 x 10-4) with BALB/cJ-derived alleles conferring increased survival. Cfw2 mapped to 58 cM on mouse Chromosome 5 and is associated with survival to weaning in female animals. Cfw2 exhibits peak linkage at D5Mit239 (P=8 x 10-6) with BALB/cJ-derived alleles conferring increased survival. Cfsw3 mapped to 37 cM on mouse Chromosome X and is associated with survival to weaning in male animals. Cfw3 spans from 29 cM - 45 cM and exhibits peak linkage at DXMit16 (P=3.1 x 10-10) with C57BL/6J-derived alleles conferring increased survival.