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Phenotypes Associated with This Genotype
Genotype
MGI:5905569
Allelic
Composition
Esrrbtm1.1Nat/Esrrbtm1.1Nat
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Esrrbtm1.1Nat mutation (1 available); any Esrrb mutation (211 available)
Tg(Myh6-cre)2182Mds mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• poor survival rates after 9-10 months of age

cardiovascular system
• increase in heart weight to body weight and heart weight to tibial length ratios
• increase in fibrosis in the left ventricle
• mice develop adult-onset dilated cardiomyopathy associated with a decrease in anterior wall thickness, increased left ventricular end systolic diameter and left ventricular end diastolic diameter and a 60% decrease in fractional shortening
• decrease in cardiac function at 9 months of age but not at 4 and 6 months, with a 60% decrease in fractional shortening
• ventricular cardiomyocytes exhibit impaired contractility and show a decrease in both contractile distance (sarcomere shortening) and speed of contraction at 6 and 9 months of age
• ventricular cardiomyocytes exhibit impaired calcium handling and deregulation of the excitation-contraction coupling apparatus
• ventricular cardiomyocytes exhibit decreased calcium release and a trend towards decreased calcium uptake as early as 4 months of age
• by 6 months of age, calcium release and uptake by ventricular cardiomyocytes are increased and this persists at 9 months
• increase in calcium transients at 6 and 9 months of age
• expression analysis indicates a heart failure gene signature in hearts

muscle
• mice develop adult-onset dilated cardiomyopathy associated with a decrease in anterior wall thickness, increased left ventricular end systolic diameter and left ventricular end diastolic diameter and a 60% decrease in fractional shortening
• decrease in cardiac function at 9 months of age but not at 4 and 6 months, with a 60% decrease in fractional shortening
• ventricular cardiomyocytes exhibit impaired contractility and show a decrease in both contractile distance (sarcomere shortening) and speed of contraction at 6 and 9 months of age
• ventricular cardiomyocytes exhibit an increase in sarcomere length only after 9 months of age

growth/size/body
• increase in heart weight to body weight and heart weight to tibial length ratios

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:241078


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
04/16/2024
MGI 6.23
The Jackson Laboratory