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:66475Genome scan at an average marker spacing of 25 cM was performed on F2 bpk/bpk animals from a (BALB/c-+/bpk x CAST/Ei)F2 intercross to identify QTLs involved with renal cystic disease severity. Bpk is a recessively inherited mutation that results in renalcystic disease. A significant QTL influencing renal cystic disease severity, Rencd (renal cystic disease severity), mapped to mouse Chromosome 6 near D6Mit14 (LOD = 5.5). CAST-derived alleles contribute to recessively inherited disease severity at Rencd. Suggestive QTLs mapped to mouse Chromosome 1 near D1Mit17 (LOD = 2.1), mouse Chromosome 2 near D2Mit72 (LOD = 1.2), mouse Chromosome 4 near D4Mit316 (LOD = 1.4), and mouse Chromosome 8 near D8Mit9 (LOD = 0.8). A possible epistatic interaction between Rencd and the locus at D1Mit17 was detected but did not reach statistical significance. |
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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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