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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Apobec2tm1Msn
targeted mutation 1, Michael S Neuberger
MGI:3701835
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Apobec2tm1Msn/Apobec2tm1Msn B6.129P2-Apobec2tm1Msn MGI:5660386
hm2
Apobec2tm1Msn/Apobec2tm1Msn involves: 129P2/OlaHsd * C57BL/6 MGI:3702511


Genotype
MGI:5660386
hm1
Allelic
Composition
Apobec2tm1Msn/Apobec2tm1Msn
Genetic
Background
B6.129P2-Apobec2tm1Msn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apobec2tm1Msn mutation (0 available); any Apobec2 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Myopathy in 8-10-month-old Apobec2tm1Msn/Apobec2tm1Msn mice

growth/size/body
• at weaning, mice of both genders have a total body mass that is ~15-20% lower than that of wild-type or heterozygous controls
• a body mass difference is evident from birth and persists until 6 months of age

muscle
• at 15 weeks of age, the proportion of soleus muscle fibers staining with an antibody against slow myosin HC increased to 40% relative to 31% in wild-type controls
• at 3 months of age, SDS-PAGE revealed an increase in the ratio of slow to fast myosin HC isoforms as shown by an increase in the proportion of type I (slow) and disappearance of type IIb isoforms
• a shift from fast to slow fibers in soleus muscle is already evident at 3 weeks of age
• at 15 weeks of age, males show a significant reduction in soleus weight relative to wild-type controls
• at 15 weeks of age, males show a significant reduction in TA weight relative to wild-type controls
• at 8-10 months of age, all muscle types examined (vastus and rectus femoris, gastrocnemius, and extensor digitorum longus) show increased variability in the size of myofibers relative to wild-type controls
• at 8-10 months of age, all muscle types examined (vastus and rectus femoris, gastrocnemius, and extensor digitorum longus) show an increased proportion of myofibers with centrally located nuclei
• a shift from fast to slow fiber types is evident in soleus muscle even in young mice
• mice older than 6 months of age develop a mild myopathy
• at 8-10 months of age, all muscle types examined display increased variability in the size of myofibers as well as an increased proportion of myofibers harboring centrally located nuclei
• however, no change is observed in the localization of laminin or dystrophin in muscle tissue

limbs/digits/tail
• at 15 weeks of age, the proportion of soleus muscle fibers staining with an antibody against slow myosin HC increased to 40% relative to 31% in wild-type controls
• at 3 months of age, SDS-PAGE revealed an increase in the ratio of slow to fast myosin HC isoforms as shown by an increase in the proportion of type I (slow) and disappearance of type IIb isoforms
• a shift from fast to slow fibers in soleus muscle is already evident at 3 weeks of age
• at 15 weeks of age, males show a significant reduction in soleus weight relative to wild-type controls
• at 15 weeks of age, males show a significant reduction in TA weight relative to wild-type controls




Genotype
MGI:3702511
hm2
Allelic
Composition
Apobec2tm1Msn/Apobec2tm1Msn
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apobec2tm1Msn mutation (0 available); any Apobec2 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are healthy and fertile, displaying no abnormalities in skeletal or cardiac muscle, up to 1 year of age





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory