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Human Disease and Mouse Model Detail
Human Disease Cardiomyopathy, Familial Hypertrophic, 10; CMH10
OMIM ID: 608758
Synonyms Cardiomyopathy, Familial Hypertrophic; Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MYL2* Myl2 View 2 models HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Myh6-MYL2*A13T)L1Dsc View 1 model
  Tg(Myh6-MYL2*D166V)1Dsc View 1 model
References Disease References using Mouse Models (2)

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
05/20/2015
MGI 5.22
The Jackson Laboratory