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 |
Tlag1 and Tlag2 appear to interact. Animals homozygous for AKR/J-derived alleles at Tlag1 and heterozygous for AKR/J- and C57L/J-derived alleles at Tlag2 exhibit the greatest susceptibility to MNU-induced lymphomas.
Mapping and Phenotype information for this QTL, its variants and associated markersJ:12885149 (AKR/J x C57L/J)F2 mice were tested for MNU induced lymphoma tumor incidence (gene Tlag1). An association between Tlag1 and the albino locus was observed in which 50% (20/40) of c/c mice developed tumors whereas only 28% (31/109) of the nonalbino (C/C or C/c) mice did so. In 135 F2 mice there was also a significant association between Hbb and tumor incidence (19/41) over Hbbd/s or Hbbs/ J:10061AKR/J mice are susceptible to MNU inducrd thymic lymphoma. The authors indicate that susceptibility is controlled by several genes. In (AKR/J x C57L/J)F2 mice one gene (Tlag1) was shown associated with the albino locus, since 6/6 albinos had tumors, and only 2/27 nonalbinos had tumors. The association of tumor incidence with the albino locus suggests tight linkage of Tlag1 and Tyrc on mouse Chromosome 7. X2 = 17.8 1 df p <.0001. |
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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 11/19/2024 MGI 6.24 |
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