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Phenotypes Associated with This Genotype
Genotype
MGI:3621567
Allelic
Composition
Erbb2tm1Cbm/Erbb2tm2Cbm
Myl2tm1(cre)Krc/Myl2+
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Erbb2tm1Cbm mutation (0 available); any Erbb2 mutation (59 available)
Erbb2tm2Cbm mutation (0 available); any Erbb2 mutation (59 available)
Myl2tm1(cre)Krc mutation (2 available); any Myl2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 27% die before reaching 6 months of age and 20% die during echochardiographic or ECG examination
• 16% die within the first 2 weeks, the rest reach adulthood

cardiovascular system
• adults and 3 month old mice exhibit myofiber hypertrophy
• frequently observe enlarged cardiomyocyte nuclei with abnormal morphology
• heart-to-body weight ratios of adults are increased by 26%, indicative of hypertrophy
• adults exhibit enlarged ventricular chambers
• seen in adults
• progressive malfunction of the heart
• at 1 month of age, see dilatation and loss of left ventricle contractility
• at 3 months of age, ventricular diameter is increased and fractional shortening is impaired
• hearts do not compensate after aortic banding but display a further decrease in fractional shortening
• significantly lengthened QTc interval caused by a slowed ventricular repolarization

muscle
• adults and 3 month old mice exhibit myofiber hypertrophy
• frequently observe enlarged cardiomyocyte nuclei with abnormal morphology
• progressive malfunction of the heart
• at 1 month of age, see dilatation and loss of left ventricle contractility
• at 3 months of age, ventricular diameter is increased and fractional shortening is impaired
• hearts do not compensate after aortic banding but display a further decrease in fractional shortening

growth/size/body
• heart-to-body weight ratios of adults are increased by 26%, indicative of hypertrophy

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:77347


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