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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    7
  • Reference
    J:27733 Nagase H, et al., Distinct genetic loci control development of benign and malignant skin tumours in mice. Nat Genet. 1995 Aug;10(4):424-9
  • ID
    MGI:45837
Genes
GeneAlleleAssay TypeDescription
Skts1 visible phenotype
D7Mit87 PCR amplified length variant MPC572
Skts2 visible phenotype
D7Mit43 PCR amplified length variant A671
Igf1r reported elsewhere
Fah reported elsewhere
Fgfr2 reported elsewhere
Hras reported elsewhere
Notes
  • Experiment
    Susceptibility to skin papillomas in mice was analyzed in a backcross panel of 326 mice derived from (NIH female x M. spretus male)F1 female mice mated back to NIH male mice. Parental strain M. spretus is resistant to skin papilloma formation compared toparental strain NIH. 133 microsatellite markers were screened. Using MAPMAKER/QTL, significant linkage (Mann-Whitney U test) of Skts1 with D7Mit87 (27.8 cM, lod 6.99) and Skts2 with D7Mit43 (64 cM, lod 5.77) was observed on mouse Chromosome 7. The linkage of Skts2 with D7Mit43 was observed in female mice only. Multiple regression analysis supports the evidence for two loci on mouse Chromosome 7. Potential candidate genes mapping near Skts1 are Igf1r (33 cM) and Fah (42.6 cM). Potential candidate genes mapping near Skts2 are Fgfr2 (63 cM) and Hras1 (72.2 cM).

Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory