
pmid: 7774920
The ky mouse mutant, kyphoscoliosis, exhibits a degenerative muscle disease resulting in chronic deformation of the spinal column. Using an interspecific backcross segregating the ky mutation, we have mapped the ky locus to a small region of mouse chromosome 9. ky is nonrecombinant with the microsatellites D9Mit24 and D9Mit169 and lies in a conserved linkage group that encompasses human chromosome 3. s-Laminin (LAMS) and the gene for dystrophin-associated glycoprotein 1 (DAG1), which map to human chromosome 3, are both recombinant with ky, ruling them out as candidates.
Genetic Markers, Membrane Glycoproteins, Base Sequence, Genetic Linkage, Molecular Sequence Data, Chromosome Mapping, Polymerase Chain Reaction, Mice, Mutant Strains, Rats, Cytoskeletal Proteins, Mice, Scoliosis, Chromosomes, Human, Pair 1, Animals, Humans, Laminin, Dystroglycans, Conserved Sequence, Crosses, Genetic, DNA Primers
Genetic Markers, Membrane Glycoproteins, Base Sequence, Genetic Linkage, Molecular Sequence Data, Chromosome Mapping, Polymerase Chain Reaction, Mice, Mutant Strains, Rats, Cytoskeletal Proteins, Mice, Scoliosis, Chromosomes, Human, Pair 1, Animals, Humans, Laminin, Dystroglycans, Conserved Sequence, Crosses, Genetic, DNA Primers
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