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Phenotypes Associated with This Genotype
Genotype
MGI:3832389
Allelic
Composition
Ldb3tm4Chen/Ldb3tm4Chen
Myl2tm1(cre)Krc/Myl2+
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ldb3tm4Chen mutation (0 available); any Ldb3 mutation (46 available)
Myl2tm1(cre)Krc mutation (2 available); any Myl2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all die between 16 and 23 weeks of age

cardiovascular system
• Z-lines in 3 month old mice are severely disrupted and disorganized and abnormal mitochondria are seen
• however M-lines are relatively normal
• enlarged left and right ventricles
• the ratios of heart weight to body weight and heart weight to tibia bone length are increased
• thinner at end diastole compared to controls
• significant increase in left ventricular dimension at end diastole and end systole
• enlarged with a thinner wall
• increase in left ventricle size is seen in mice at 2 - 4 months of age but not at 1 month of age
• enlarged with a thinner wall
• in both the left and right ventricles
• electrocardiography reveals an atrioventricular block

muscle
• Z-lines in 3 month old mice are severely disrupted and disorganized and abnormal mitochondria are seen
• however M-lines are relatively normal

growth/size/body
• enlarged left and right ventricles
• the ratios of heart weight to body weight and heart weight to tibia bone length are increased

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy 1C DOID:0110423 OMIM:601493
J:144739


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
11/12/2024
MGI 6.24
The Jackson Laboratory