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Phenotypes Associated with This Genotype
Genotype
MGI:3716195
cx31
Allelic
Composition
Dmdmdx/?
Fgf6tm1Thbr/Fgf6tm1Thbr
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/10ScSn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdmdx mutation (31 available); any Dmd mutation (156 available)
Fgf6tm1Thbr mutation (0 available); any Fgf6 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• dorso-ventral curvature of the spine

muscle
N
• no clinical signs of severe dystrophy for up to 6 months
• back and body wall musculature show changes similar to diaphragm but less uniformly and more focally distributed
• muscle changes similar to diaphragm but less uniformly and more focally distributed
• pronounced increase in collagen
• increase in mononuclear cells
• unusually small myotubes with very few centrally located nuclei
• changes are not enhanced compared to Dmd mutants
• severe myopathy observed in diaphragm, limb muscles, and back muscles


Contributing Projects:
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
03/18/2025
MGI 6.24
The Jackson Laboratory