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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    2
  • Reference
    J:73581 Cho HY, et al., Linkage Analysis of Susceptibility to Hyperoxia. Nrf2 is a candidate gene. Am J Respir Cell Mol Biol. 2002 Jan 1;26(1):42-51
  • ID
    MGI:2389120
Genes
GeneAlleleAssay TypeDescription
Hsl1 resistance/susceptibility
D2Mit271
D2Mit476
Nfe2l2 reported elsewhere
Notes
  • Experiment
    Linkage analysis was performed on (C57BL/6J x C3H/HeJ)F2 intercross animals and BXH RI strains to identify QTLs associated with susceptibility to hyperoxia. Parental strain C57BL/6J is susceptible to hyperoxia whereas C3H/HeJ is resistant. A locus named Hsl1, hyperoxia susceptibility locus 1, mapped to 48 cM on mouse Chromosome 2 in linkage to polymorphonuclear leukocyte (PMN) infiltration with LRS=13.2 at D2Mit248. Hsl1 is also linked to hyperoxia-induced changes in endothelial cell and macrophage levels. The QTL range of Hsl1 spans 45 cM - 49.2 cM on chromosome 2. C57BL/6J-derived alleles confer susceptibility to hyperoxia at this locus. A strong candidate gene for Hsl1 is Nfe2l2. Basal mRNA level of Nfe2l2 is 1.8-fold higher in C3H/HeJ animals compared to C57BL/6J, and the difference increases following hyperoxic lung injury. Sequence analysis detected a T to C substitution in the Nfe2l2 promoter region (position -336) in C57BL/6J, and the polymorphism was shown to segregate with the phenotype. A suggestive QTL, Hsl2, mapped from 51.1 cM - 58.5 cM on mouse Chromosome 3.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory