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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CAMalpha1b)7Wjk
transgene insertion 7, Walter Koch
MGI:1858099
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(CAMalpha1b)7Wjk/? Not Specified MGI:3800634


Genotype
MGI:3800634
tg1
Allelic
Composition
Tg(CAMalpha1b)7Wjk/?
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(CAMalpha1b)7Wjk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• the heart to body weight ratio is increased by 20% compared to non-transgenic controls
• approximate 2.5-fold increase in heart weight, suggesting eccentric cardiac hypertrophy in the late stages of cardiomyopathy
• myocytes located in the right ventricle have a 62% higher cross-section than found in non-transgenic controls

mortality/aging
• average age of death is 8.6 +/- 0.7 months
• males survive longer than females, dying on average at 12.4 months compared to 7 months for females

cardiovascular system
N
• systolic and diastolic blood pressure is normal in these mice
• heart muscle contains elevated levels of diacylglycerol resulting from enhanced signaling by the alpha 1 adrenergic receptor through the Gq-phospholipase C-protein kinase C signaling pathway
• left ventricular walls exhibit myofibrillar disarray
• distortion of both ventricles
• the heart to body weight ratio is increased by 20% compared to non-transgenic controls
• approximate 2.5-fold increase in heart weight, suggesting eccentric cardiac hypertrophy in the late stages of cardiomyopathy
• myocytes located in the right ventricle have a 62% higher cross-section than found in non-transgenic controls
• left ventricular end-systolic area and left ventricular end-diastolic area are higher at 6 and 9 months of age but not at 3 months, indicating progressive left ventricle enlargement with age
• all 4 cardiac chambers are enlarged
• however, posterior and septum wall thickness are largely unchanged
• mice exhibit late-onset dilated cardiomyopathy
• fractional area change is decreased between 3 and 9 months of age by about 20%, indicating loss in left ventricular systolic function
• left ventricular end-systolic area and left ventricular end-diastolic area are higher at 6 and 9 months of age but not at 3 months, indicating progressive left ventricle enlargement with age
• left ventricular end-systolic area is increased over 80% from 3 to 9 months of age
• fractional area change is decreased between 3 and 9 months of age by about 20%
• mice present with signs of heart failure, including fatigue and dyspnea, followed by generalized edema and death

homeostasis/metabolism
• frequent presence of right atrial thrombus
• seen before mice die

muscle
• heart muscle contains elevated levels of diacylglycerol resulting from enhanced signaling by the alpha 1 adrenergic receptor through the Gq-phospholipase C-protein kinase C signaling pathway
• left ventricular walls exhibit myofibrillar disarray
• myocytes located in the right ventricle have a 62% higher cross-section than found in non-transgenic controls
• mice exhibit late-onset dilated cardiomyopathy
• fractional area change is decreased between 3 and 9 months of age by about 20%, indicating loss in left ventricular systolic function

respiratory system
• seen before mice die

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:134704





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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
11/19/2024
MGI 6.24
The Jackson Laboratory