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 |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:125558Previously mapped loci influencing survival in Cftrtm1Unc mice on chromosomes 3, 5, and X were investigated using an expanded population of 1208 (C57BL/6-Cftrtm1Unc x BALB/cJ)F2 animals. Of the 1208 F2 animals, 137 were homozygous for the Cftrtm1Uncmutation, which is fewer than the 25% predicted for an autosomal recessive trait. Analysis of 186 F2 embryos at E15.5 revealed the expected Mendelian segregation ratios for Cftrtm1Unc homozygous, heterozygous, and wild type genotypes. Authors conclude early lethality for Cftr1tm1Unc homozygous animals occurs between E15.5 and 3-weeks post-weaning. Female-specific transmission ratio distortion mapping to 37 cM on mouse Chromosome X was verified in this study. An excess of BALB/cJ alleles is observed at DXMit16 in 3-week old non-CF female F2 animals. This locus is named Tmrdq1 (transmission ratio distortion QTL 1). Potential candidate genes in this region include Arx (33.9 cM) and Nr0b1 (formerly Dax1, 33 cM). Female-specific transmission ratio distortion was confirmed on mouse Chromosome 5 near D5Mit239 (58 cM). This locus is named Tmrdq2 (transmission ratio distortion QTL 2). An excess of BALB/cJ alleles is observed at Tmrd2 in 3-week old non-CF female F2 animals. The chromosome 3 locus for transmission ratio distortion was not replicated in this study. |
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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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