About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3691280
Allelic
Composition
Myh6tm1Ces/Myh6tm1Ces
Genetic
Background
involves: 129S/SvEv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myh6tm1Ces mutation (0 available); any Myh6 mutation (206 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• progress rapidly to dilated cardiomyopathy, however do not exhibit myofibrillar disarray or fibrosis
• develop contractile dysfunction and reduced fractional shortening at around 12 weeks of age

muscle
• progress rapidly to dilated cardiomyopathy, however do not exhibit myofibrillar disarray or fibrosis
• develop contractile dysfunction and reduced fractional shortening at around 12 weeks of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:114549


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory