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Phenotypes Associated with This Genotype
Genotype
MGI:4881929
Allelic
Composition
Actg1tm1.2Erv/Actg1tm1.2Erv
Tg(ACTA1-cre)79Jme/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Actg1tm1.2Erv mutation (1 available); any Actg1 mutation (23 available)
Tg(ACTA1-cre)79Jme mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• about 2/3 of mice show classical hind limb contractures when suspended by the tail
• persists throughout life without getting any worse
• reduced mobility
• persists throughout life without getting any worse

muscle
• dystrophin is less organized at the z-line in some muscles
• muscles primarily made up of type II fibers are most affected
• more variability in muscle fiber size
• centrally nucleated fibers start appearing in muscle at about 3 months of age and progress to widespread incidence by 12 to 18 months
• maximal force production by extensor digitorum longus muscle is less than in controls
• maximal titanic force is similar to controls


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
04/30/2024
MGI 6.23
The Jackson Laboratory