Summary |
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Variant origin |
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Variant description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Notes |
Animals homozygous for B10.O20/Dem-derived alleles at Sluc15 and homozygous for O20/A-derived alleles at Sluc23 exhibit decreased lung tumor size.
Sluc23 and Sluc30 interact. Heterozygosity at Sluc23 and homozygosity for O20/A-derived alleles at Sluc30 confers increased lung tumor size. Mapping and Phenotype information for this QTL, its variants and associated markersJ:71973Several F2 crosses between inbred strain O20/A and recombinant congenic strains OcB-3/Dem, OcB-4/Dem, OcB-6/Dem, OcB-9/Dem, and OcB-16/Dem were used to map QTLs linked to lung tumor susceptibility. Parental strain O20/A and OcB-4/Dem are susceptible to lung tumor development after ENU treatment whereas parental strains OcB-3/Dem, OcB-6/Dem, OcB-9/Dem, and OcB-16/Dem are relatively resistant. 14 previously identified lung tumor susceptibility loci were detected in these crosses (Sluc1-Sluc14) and 16 new loci were identified with a statistical significance of P>0.05. All of the QTL were detected in pairwise interactions, Table 1, Fig 1. In the (OcB3 x O20/A)F2 cross a newly identified QTL, Sluc23, mapped to mouse Chr 13 in linkage with D13Mit139 at approximately 32 cM. |
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References |
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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 11/12/2024 MGI 6.24 |
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