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Phenotypes Associated with This Genotype
Genotype
MGI:3616711
Allelic
Composition
Mdm4tm2Glo/Mdm4tm2.1Glo
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mdm4tm2.1Glo mutation (0 available); any Mdm4 mutation (193 available)
Mdm4tm2Glo mutation (1 available); any Mdm4 mutation (193 available)
Tg(Myh6-cre)2182Mds mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• some mice die within 1 year for unknown reasons, however do not observe any embryonic lethality (J:104114)
• median survival of 208 and 243 days for males and females, respectively (J:137114)
• mice die as a result of heart failure (J:137114)

cellular

cardiovascular system
N
• no abnormalities in embryonic hearts are seen
• hearts exhibit half the number of cardiomyocytes at 8 months of age
• marker analysis indicates cardiomyocyte hypertrophy
• ventricular walls are thinner and hypertrophic
• all 4 chambers are dilated and paler than control hearts
• severe dilated cardiomyopathy
• by 8-10 months of age, most mice have swollen bodies, have difficulty moving, and are out of breath

homeostasis/metabolism
• edema in the lung and/or abdomen

muscle
• hearts exhibit half the number of cardiomyocytes at 8 months of age
• marker analysis indicates cardiomyocyte hypertrophy
• severe dilated cardiomyopathy

growth/size/body

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:137114


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
12/10/2024
MGI 6.24
The Jackson Laboratory