Summary |
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Variant origin |
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Variant description |
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Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:90096Genome scan using 83 polymorphic markers across chromosomes 2-19 at an average resolution of 20 cM was performed on 152 (C57BL/6J-En1tm1Alj x 129S1)F2 animals and 74 (C57BL/6J-En1tm1Alj x 129S1)F1 x C57BL/6J-En1tm1Alj backcross animals to identifyQTLs modifying limb development. The En1tm1Alj mutation exhibits variable severity depending on strain background. Forelimb polydactyly is more prevalent among C57BL/6J-En1tm1Alj homozygotes whereas syndactyly, cartoon paw, and preaxial shift are more prevalent among 129S1-En1tm1Alj homozygotes. Significant linkage to hindlimb polydactyly mapped to distal mouse Chromosome 2 between D2Mit311 (83.1 cM, LOD=5) and D2Mit229 (99 cM, LOD=4). This locus is named Hpdty (hindlimb polydactyly). 129S1-derived alleles appear to confer increased incidence of hindlimb polydactyly with a dominant mode of inheritance. Bmp2 and Bmp7 map within the Hpdty region and are considered candidate genes. Previous studies with Bmp7-deficient mutants results in preaxial polydactyly of the hindlimbs. Also, SNPs between C57BL/6J and 129S1 exist in the intronic regions of Bmp2 and Bmp7.Linkage to preaxial shift (Prxsh) mapped to 37 cM on mouse Chromosome 8 near D8Mit104 (LOD=3.1). This locus also shows suggestive linkage to 2/3syndactyly (LOD=2.2). Also on mouse Chromosome 8, forelimb polydactyly (Fpdty) mapped to 53 cM near D8Mit271 (LOD=3.3).Linkage to type I polydactyly (T1pdty) mapped to 56.7 cM on mouse Chromosome 17 near D17Mit123 (LOD=3.1). |
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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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