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Phenotypes Associated with This Genotype
Genotype
MGI:7571248
Allelic
Composition
Dsg2em1Spin/Dsg2em1Spin
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dsg2em1Spin mutation (0 available); any Dsg2 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased ICD volume in heart owing to increased width between cells
• pale embryos with blood accumulation around heart at stage E12.5
• deformed
• fibrotic and calcified areas in myocardium
• hypertrophic cardiomyocytes
• fibrotic and calcified areas in myocardium
• fibrotic and calcified areas in myocardium
• in E12.5 embryos
• reduced tricuspid annular plane systolic excursion and fractional shortening
• reduced fractional shortening
• reduced tricuspid annular plane systolic excursion and fractional shortening
• ventricular arrhythmia
• increased QRS interval
• decreased S peak amplitude

cellular
• widened intercellular space in myocardium with some ruptured cell-cell junctions

growth/size/body

homeostasis/metabolism
• in E12.5 embryos

integument

mortality/aging
• most embryos die by stage E14
• mice born at a fraction of expected Mendelian ratio

muscle
• increased ICD volume in heart owing to increased width between cells
• reduced tricuspid annular plane systolic excursion and fractional shortening

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
intrinsic cardiomyopathy DOID:0060036 J:342765


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
11/05/2024
MGI 6.24
The Jackson Laboratory