Assuntos
Mutação , Polidactilia/genética , Sindactilia/genética , Dedos do Pé/anormalidades , Animais , Cruzamentos Genéticos , Feminino , Heterozigoto , Homozigoto , Deformidades Congênitas dos Membros/genética , Masculino , Camundongos , Camundongos Endogâmicos C3H , Fenótipo , Recombinação GenéticaRESUMO
Preaxial polydactyly is a congenital hand malformation that includes duplicated thumbs, various forms of triphalangeal thumbs, and duplications of the index finger. A locus for preaxial polydactyly has been mapped to a region of 1.9 cM on chromosome 7q36 between polymorphic markers D7S550 and D7S2423. We constructed a detailed physical map of the preaxial polydactyly candidate region. With a combination of methods we identified and positioned 11 transcripts within this map. By recombination analysis on families with preaxial polydactyly, using newly developed polymorphic markers, we were able to reduce the candidate region to approximately 450 kb. The homeobox gene HLXB9, a putative receptor C7orf2, and two transcripts of unknown function, C7orf3 and C7orf4, map in the refined candidate region and have been subjected to mutation analysis in individuals with preaxial polydactyly.
