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Phenotypes Associated with This Genotype
Genotype
MGI:5910392
Allelic
Composition
Ppp1r13ltm1.1Xlu/Ppp1r13ltm1.1Xlu
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppp1r13ltm1.1Xlu mutation (0 available); any Ppp1r13l mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice show a more rapid mortality beginning at 10 weeks of age, with a median survival of 40 weeks
• mice die of sudden cardiac death without signs of prior illness

cardiovascular system
• loss of cardiac muscle in the right ventricular wall
• accumulation of fat droplets is only seen at sites of fibrosis in all hearts
• E16.5 and E18.5 hearts show severe disruption of the myocardial structure, with a variegated pattern of muscle damage
• loss of myocardial integrity that includes the interventricular septum is seen by E18.5
• interaction between the desmin-containing intermediate filaments is disrupted in desmosomes
• intercalated discs of cardiomyocytes show abnormal distribution of proteins
• 12 week old mice show irregularly shaped intercalated discs with widened gaps between the two-electron dense desmosomal plates
• myocardial disarray and increased intercellular spaces between myocytes in myocardial regions
• E16.5 and E18.5 hearts show erosion and thinning of the right ventricular wall
• both the left and right ventricles are dilated in 12 week old mice
• right ventricular dilation in E16.5 hearts
• in 12 week old mice
• in 12 week old mice
• increase in end-systolic volumes and decrease in ventricular ejection fraction at 12 weeks of age
• contraction of the ventricles is minimal as indicated by minimal change in the cross-sectional area between end-diastolic and end-systolic frames at midpapillary level
• increase in end-systolic volumes and decrease in stroke volume, ventricular ejection fraction, and cardiac output at 12 weeks of age
• young adult mice show frequent spontaneous runs of nonsustained ventricular tachycardia
• young adult mice show frequent multifocal ventricular ectopy
• heart exhibit features of human arrhythmogenic right ventricular cardiomyopathy

homeostasis/metabolism
• blood clots are seen in E16.5 and E18.5 hearts

muscle
• E16.5 and E18.5 hearts show severe disruption of the myocardial structure, with a variegated pattern of muscle damage
• loss of myocardial integrity that includes the interventricular septum is seen by E18.5
• interaction between the desmin-containing intermediate filaments is disrupted in desmosomes
• intercalated discs of cardiomyocytes show abnormal distribution of proteins
• 12 week old mice show irregularly shaped intercalated discs with widened gaps between the two-electron dense desmosomal plates
• myocardial disarray and increased intercellular spaces between myocytes in myocardial regions
• loss of cardiac muscle in the right ventricular wall
• increase in end-systolic volumes and decrease in ventricular ejection fraction at 12 weeks of age
• contraction of the ventricles is minimal as indicated by minimal change in the cross-sectional area between end-diastolic and end-systolic frames at midpapillary level
• heart exhibit features of human arrhythmogenic right ventricular cardiomyopathy

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
arrhythmogenic right ventricular cardiomyopathy DOID:0050431 OMIM:PS107970
J:220162


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