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Human Disease and Mouse Model Detail
Human Disease Cardiomyopathy, Familial Hypertrophic, 2; CMH2
OMIM ID: 115195
Human Phenotype Ontology associations
Synonyms Cardiomyopathy, Familial Hypertrophic
View all models View ALL (6) 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
     TNNT2* Tnnt2* View 6 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-Tnnt2)117Lnwd View 1 model
  Tg(Myh6-Tnnt2)191Lnwd View 1 model
  Tg(Myh6-Tnnt2*R92Q)2Lnwd View 1 model
  Tg(Myh6-TNNT2*R92Q)#Ajm View 1 model
  Tg(Tnnt2-TNNT2*R92Q)#Ajm View 1 model
  Tg(Tnnt2-TNNT2*R92Q)M-2Ajm View 1 model
References Disease References using Mouse Models (6)

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
MGI 6.07
The Jackson Laboratory