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Phenotypes Associated with This Genotype
Genotype
MGI:6118901
Allelic
Composition
Hspb7tm1.1Yty/Hspb7tm1.1Yty
Tg(ACTA1-cre)79Jme/0
Genetic
Background
involves: 129 * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hspb7tm1.1Yty mutation (0 available); any Hspb7 mutation (14 available)
Tg(ACTA1-cre)79Jme mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all mice die between P1 and P60
• mice start to die within the first week after birth

muscle
• disorganized the diaphragm at 6 months, including sarcomeric Z- line streaming, the insertion of an additional sarcomere, and myofibrillar disorganization with focal loss of cross-striation
• Z-line streaming, causing filament disruption, and Z-line disruption are observed in the diaphragm muscle
• at 36 weeks in diaphragm muscles
• fibrosis at 12 weeks
• disorganized sarcomeres in the diaphragm at 6 months, including sarcomeric Z-line streaming, the insertion of an additional sarcomere, and myofibrillar disorganization with focal loss of cross-striation
• diaphragm muscle exhibits filament disruption, small rod bodies and vacuoles and central nuclei
• irreversible aggregation of filamin C and sarcoglycans
• reduced muscle mass with reduced muscle weight at 12 weeks
• however, diaphragm is normal at P1
• in the diaphragm, but not the soleus, at 2 weeks
• progressive

respiratory system
• elevated enhanced pause
• increased respiratory peak expiration flow and relaxation time at lower breath frequency

homeostasis/metabolism

growth/size/body
• after 40 weeks

behavior/neurological
• at 36 weeks with progressive myopathy


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
01/28/2026
MGI 6.24
The Jackson Laboratory