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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Myh6-Gnaq*Q209L)44Ejne
transgene insertion 44, EJ Neer
MGI:5905048
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne involves: FVB MGI:5905050
tg2
Tg(Myh6-Gnaq*Q209L)44Ejne/0 involves: FVB MGI:5905051


Genotype
MGI:5905050
tg1
Allelic
Composition
Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne
Genetic
Background
involves: FVB
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
homeostasis/metabolism
• left atria often contains thombi

mortality/aging
• mice die prematurely at 12-14 months of age

cardiovascular system
• enlarged cardiac myocytes contain big hyperchromatic nuclei, intracellular vacuolization, and interstitial fibrosis
• the right atrial weight is elevated by 12 months of age
• the left atria is enlarged by 12 months of age and left atrial diameter is increased by about 50%
• the ventricular weight/body weight ratio is increased
• a group of 12-14 month old mice exhibit dilated ventricles and increased ventricle weight
• a group of 12-14 month old mice exhibit dilated ventricles and increased ventricle weight while a subset of mice at this age do not show increased ventricular mass and dilation
• enlarged cardiac myocytes exhibit interstitial fibrosis
• the 4 chambers of 12.5 month old hearts are enlarged
• age of onset of dilated cardiomyopathy ranges between 11 and 13 months of age and the phenotype progresses to end-stage dilation with a concomitant reduction in fractional shortening within 2-3 months
• however, left ventricular wall thickness remains unchanged indicating no initial hypertrophic response
• decrease in systolic contractile function, with a reduction in fractional shortening below 15%
• M-mode and echocardiography show increases in left ventricular end-systolic and end-diastolic diameters at 12-14 months of age
• heart rates are slower in anaesthetized mice and in conscious mice during blood pressure recordings
• mice show signs of left and right heart failure at end-stage

muscle
• enlarged cardiac myocytes contain big hyperchromatic nuclei, intracellular vacuolization, and interstitial fibrosis
• the 4 chambers of 12.5 month old hearts are enlarged
• age of onset of dilated cardiomyopathy ranges between 11 and 13 months of age and the phenotype progresses to end-stage dilation with a concomitant reduction in fractional shortening within 2-3 months
• however, left ventricular wall thickness remains unchanged indicating no initial hypertrophic response
• decrease in systolic contractile function, with a reduction in fractional shortening below 15%

cellular
• enlarged cardiac myocytes exhibit interstitial fibrosis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:127756




Genotype
MGI:5905051
tg2
Allelic
Composition
Tg(Myh6-Gnaq*Q209L)44Ejne/0
Genetic
Background
involves: FVB
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
mortality/aging
• mice die around 18-19 months of age often with signs of left and right heart failure

cardiovascular system
• hemizygous mice develop the same cardiac phenotypes as homozygotes that lead to dilated cardiomyopathy but about 5-6 months later than homozygotes
• mice show signs of left and right heart failure at 18-19 months of age

muscle
• hemizygous mice develop the same cardiac phenotypes as homozygotes that lead to dilated cardiomyopathy but about 5-6 months later than homozygotes

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:127756





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory