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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Emdtm1.1Stw
targeted mutation 1.1, Colin L Stewart
MGI:3621266
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Emdtm1.1Stw/Emdtm1.1Stw involves: 129S1/Sv * FVB/N MGI:3621375
ot2
Emdtm1.1Stw/Y involves: 129S1/Sv * C57BL/6 MGI:5912138
ot3
Emdtm1.1Stw/Y involves: 129S1/Sv * FVB/N MGI:3621419


Genotype
MGI:3621375
hm1
Allelic
Composition
Emdtm1.1Stw/Emdtm1.1Stw
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emdtm1.1Stw mutation (1 available); any Emd mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
N
• no signs of muscular atrophy or dystrophy or cardiac pathology up to 1 year of age

cellular
N
• nuclear morphology was normal and other nuclear envelop proteins are normally distributed




Genotype
MGI:5912138
ot2
Allelic
Composition
Emdtm1.1Stw/Y
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emdtm1.1Stw mutation (1 available); any Emd mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increase in number of small and reduction in number of large cardiomyocytes
• increase of mononucleated and a decrease of multinucleated cardiomyocytes
• reduction in size of cardiomyocytes
• increase in the number of cardiomyocytes in 5 week old hearts
• however, size and left ventricular mass of hearts is normal
• slight, but significant, increase in heart weight to tibia length ratio
• increase in levels of cardiac stress markers ANP and BNP
• however, no cardiac fibrosis is seen
• lower ejection fraction of both the right and left ventricles
• increase in end-diastolic and end-systolic volumes in mice and lower ejection fraction of both the right and left ventricles
• mice exhibit a decline of ejection fraction and increase of end-systolic volume 3- and 6- months after transverse aortic constriction (TAC) indicating impaired response to pressure overload
• marker analysis indicates increased cardiac remodeling in hearts after TAC
• however, no effect on left ventricular mass after TAC is seen

homeostasis/metabolism
• mice exhibit a decline of ejection fraction and increase of end-systolic volume 3- and 6- months after transverse aortic constriction (TAC) indicating impaired response to pressure overload
• marker analysis indicates increased cardiac remodeling in hearts after TAC
• however, no effect on left ventricular mass after TAC is seen

muscle
• increase in number of small and reduction in number of large cardiomyocytes
• increase of mononucleated and a decrease of multinucleated cardiomyocytes
• reduction in size of cardiomyocytes
• increase in the number of cardiomyocytes in 5 week old hearts
• however, size and left ventricular mass of hearts is normal
• lower ejection fraction of both the right and left ventricles

growth/size/body
• slight, but significant, increase in heart weight to tibia length ratio




Genotype
MGI:3621419
ot3
Allelic
Composition
Emdtm1.1Stw/Y
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emdtm1.1Stw mutation (1 available); any Emd mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• after muscle degeneration resulting from cardiotoxin injection,myofiber regeneration is slower
• smaller diameter at 7 days, similar to 3 day controls
• fiber diameter more heterogeneous
• 14 day animals similar to controls except for increased variability in fiber diameter
• delayed differentiation of myoblasts in culture
• no signs of muscular atrophy or dystrophy or cardiac pathology up to 1 year of age

cellular
N
• nuclear morphology was normal and other nuclear envelop proteins are normally distributed

limbs/digits/tail
• after muscle degeneration resulting from cardiotoxin injection,myofiber regeneration is slower
• smaller diameter at 7 days, similar to 3 day controls
• fiber diameter more heterogeneous
• 14 day animals similar to controls except for increased variability in fiber diameter
• delayed differentiation of myoblasts in culture
• no signs of muscular atrophy or dystrophy or cardiac pathology up to 1 year of age





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory