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Phenotypes Associated with This Genotype
Genotype
MGI:3608495
Allelic
Composition
Mybpc3tm1Lcrr/Mybpc3+
Genetic
Background
involves: 129S4/SvJae * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mybpc3tm1Lcrr mutation (0 available); any Mybpc3 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• mutant mice develop asymmetric septal hypertrophy associated with fibrosis at 10-11 month of age

Mouse Models of Human Disease
OMIM ID Ref(s)
Cardiomyopathy, Familial Hypertrophic, 4; CMH4 115197 J:101903


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/17/2016
MGI 6.05
The Jackson Laboratory