Reference : Rbt (Rabo torcido), a new mouse skeletal mutation involved in anteroposterior pattern...
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/10993/1303
Rbt (Rabo torcido), a new mouse skeletal mutation involved in anteroposterior patterning of the axial skeleton, maps close to the Ts (tail-short) locus and distal to the Sox9 locus on chromosome 11.
English
Hustert, E. [> >]
Scherer, G. [> >]
Olowson, M. [> >]
Guenet, J. L. [> >]
Balling, Rudi mailto []
1996
Mammalian Genome : Official Journal of the International Mammalian Genome Society
7
12
881-5
Yes (verified by ORBilu)
0938-8990
1432-1777
UNITED STATES
[en] Animals ; Body Patterning/genetics ; Bone and Bones/abnormalities ; Chromosome Mapping ; Female ; High Mobility Group Proteins/genetics ; Male ; Mice ; Mice, Inbred C57BL ; SOX9 Transcription Factor ; Tail ; Transcription Factors/genetics ; Transformation, Genetic
[en] Rbt (Rabo torcido) is a new semidominant mouse mutant with a variety of skeletal abnormalities. Heterozygous Rbt mutants display homeotic anteroposterior patterning problems along the axial skeleton that resemble Polycomb group and trithorax gene mutations. In addition, the Rbt mutant displays strong similarities to the phenotype observed in Ts (Tail-short), indicating also a homeotically transformed phenotype in these mice. We have mapped the Rbt locus to an interval of approximately 6 cM on mouse Chromosome (Chr) 11 between microsatellite markers D11Mit128 and D11Mit103. The Ts locus was mapped within a shorter interval of approximately 3 cM between D11Mit128 and D11Mit203. This indicates that Rbt and Ts may be allelic mutations. Sox9, the human homolog of which is responsible for the skeletal malformation syndrome campomelic dysplasia, was mapped proximal to D11Mit128. It is, therefore, unlikely that Ts and Rbt are mouse models for this human skeletal disorder.
http://hdl.handle.net/10993/1303

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