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Phenotypes Associated with This Genotype
Genotype
MGI:3722314
Allelic
Composition
Dmdtm1Mok/Y
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdtm1Mok mutation (2 available); any Dmd mutation (154 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• at 4 and 4.5 months of age, the diaphragm exhibits an increase in connective tissue
• at 4 and 4.5 months of age, dissected muscles are whitish and hypertrophic
• several muscles exhibit an increase in size and an increase in connective tissue with necrotic fibers
• muscle degeneration is similar to that observed in other Dmd deficient mice

cellular
• in the plasma membrane of the extensor digitorum longus, caveola density is increased while the density of intramembranous particles is decreased

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Duchenne muscular dystrophy DOID:11723 OMIM:310200
J:43164


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
11/05/2024
MGI 6.24
The Jackson Laboratory