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 |
J:29366 penetrance of ct mutation (versus 38% on STOCK): C57BL/6J (18.50%), BXD-8/Ty (17.73%), BALB/cByJ (7.90%), M. spretus (2.50%), CAST/Ei (0%) and MOLF/Ei (0%).
Mapping and Phenotype information for this QTL, its variants and associated markersJ:29366(M. spretus x STOCK-ct/ct)F1 x STOCK-ct/ct and (BALB/cByJ x STOCK-ct/ct)F1 x STOCK-ct/ct interspecific backcross progeny were genotyped using 70 SSCP markers on 19 autosomes in a genome wide scan in an attempt to identify loci which modify the ct (curly tail) phenotype. Curly tail is coded for by a locus on mouse Chromosome 4. Various statistical parameters were used to identify a region of mouse Chromosome 17 that modified the ct phenotype. Authors have named this recessive locus mct1, modifier of curly-tail 1. By combining progeny from the two backcrosses an order of loci on mouse Chromosome 17 was indicated as: D17Mit113 - D17Mit134 - mct1 - D17Mit11 - D17Mit6 - D17Mit3 - D17Mit72 - D17Mit123. |
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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 12/10/2024 MGI 6.24 |
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