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Phenotypes Associated with This Genotype
Genotype
MGI:3688755
Allelic
Composition
Tg(Myh6-Myl2*)21Rbns/0
Genetic
Background
Not Specified
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phenotype observed in females
phenotype observed in males
N normal phenotype

Abnormal cardiac structure in Tg(Myh6-Myl2*)21Rbns/0 mice

cardiovascular system
• cardiomyocytes are irregularly shaped, show the presence of vacuoles, have an irregular distribution of mitochondria and develop myofibril degeneration
• sarcomeric organization is lost, the intercalated discs are convoluted, large interstitial spaces separate the myocytes and there is increased collagen deposition
• intercalated discs are convoluted in cardiomyocytes
• cardiomyoctyes develop myofibril degeneration
• biatrial hypertrophy
• show a trend toward septal hypertrophy at 10 weeks of age, however left ventricle free wall weights are unaffected
• exhibit biatrial hypertrophy, a trend toward septal hypertrophy and activation of hypertrophic markers
• seen at 16 weeks of age
• the response of dP/dtmax to beta-adrenergic stimulation is significantly reduced, although heart rate is not affected
• perfused hearts consistently show decreased contractility throughout the range of frequencies tested, however show no differences in the force-frequency relation in papillary muscles, the pressure-frequency relation in Langendorff perfused hearts, or shortening-frequency relation of isolated cardiac myocytes
• the absolute values of dP/dtmin are lower under both nonstimulated conditions and at all levels of beta-adrenergic stimulation, however no differences are seen in mean arterial pressure and left ventricular end diastolic pressure
• severe tricuspid valve insufficiency as evidenced by the regurgitation jet in 16 week old mutants
• perfused hearts show a reduction in left ventricular developed pressure of about 20 mmHg at the median frequency (450 bpm) tested
• force production of fibers in response to increasing calcium levels is normal under dephosphorylated conditions, however after myosin light chain kinase treatment to induce phosphorylation, mutants do not show an increase in calcium sensitivity (no leftward shift in the force-calcium curve) as is seen in controls
• perfused hearts consistently develop a reduced systolic pressure at all the frequencies of stimulation tested

muscle
• cardiomyocytes are irregularly shaped, show the presence of vacuoles, have an irregular distribution of mitochondria and develop myofibril degeneration
• sarcomeric organization is lost, the intercalated discs are convoluted, large interstitial spaces separate the myocytes and there is increased collagen deposition
• intercalated discs are convoluted in cardiomyocytes
• cardiomyoctyes develop myofibril degeneration
• the response of dP/dtmax to beta-adrenergic stimulation is significantly reduced, although heart rate is not affected
• perfused hearts consistently show decreased contractility throughout the range of frequencies tested, however show no differences in the force-frequency relation in papillary muscles, the pressure-frequency relation in Langendorff perfused hearts, or shortening-frequency relation of isolated cardiac myocytes
• the absolute values of dP/dtmin are lower under both nonstimulated conditions and at all levels of beta-adrenergic stimulation, however no differences are seen in mean arterial pressure and left ventricular end diastolic pressure
• sarcomere organization in lost in cardiomyocytes

growth/size/body
• exhibit biatrial hypertrophy, a trend toward septal hypertrophy and activation of hypertrophic markers


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