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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Myh6-MYL2*D94A)1Dsc
transgene insertion 1, Danuta Szczesna-Cordary
MGI:6193897
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Myh6-MYL2*D94A)1Dsc/0 Not Specified MGI:6193898


Genotype
MGI:6193898
tg1
Allelic
Composition
Tg(Myh6-MYL2*D94A)1Dsc/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• myopathic vacuolar formations in the myocardium of 9 month old mice
• mice exhibit biventricular cardiac dilation by about 5 months of age
• left ventricle chamber dilation in young males and in both males and females at 12 months of age
• only mild fibrosis is seen in older male hearts
• however, no myofilament disarray or extensive fibrosis is seen in left ventricular tissue from 5 and 12 month old mice
• hemodynamic assessment and pressure-volume loop analysis shows decreased intact heart function in young and old mice
• diminished cardiac function is more severe in males than in females
• young and old mice show elevated arterial elastance
• mice exhibit decreased stroke work and prerecruitable stroke work decreased cardiac output MP:0003393
• mice develop progressive dilated cardiomyopathy by 12 months of age
• severely reduced ejection fraction and fractional shortening in younger and older mice
• elevated end-systolic and end-diastolic volume
• however, mice do not exhibit diastolic dysfunction
• echocardiography shows that mice develop diminished cardiac function as heart chamber size increases
• skinned and intact papillary muscle fibers exhibit abnormalities in myofilament contractility, with decrease in calcium sensitivity of force, reduced contractile force at submaximal calcium concentrations and faster (shorter time) relaxation phase of force transients
• cardiac myosin purified from ventricles shows hypocontractile activity reflecting a diminished ability of myosin to hydrolize ATP to produce energy for muscle contraction
• papillary muscle fibers exhibit less association of myosin heads with thin filaments

muscle
• myopathic vacuolar formations in the myocardium of 9 month old mice
• mice develop progressive dilated cardiomyopathy by 12 months of age
• severely reduced ejection fraction and fractional shortening in younger and older mice
• elevated end-systolic and end-diastolic volume
• however, mice do not exhibit diastolic dysfunction
• hearts exhibit disrupted sarcomeric structures

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:258888





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