About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Myotonic Dystrophy 1; DM1
OMIM ID: 160900
Synonyms Dystrophia Myotonica 1; Dystrophia Myotonica; DM; Myotonic dystrophy; Steinert Disease
View all models View ALL (17) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Dmpk* DMPK* View 2 models 1:1 Homology
     Mbnl1* MBNL1 View 1 model 1:1 Homology
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(CAG-DMPK*)1323Coop View 2 models
  Tg(Ckm-CUGBP1)1039Coop View 1 model
  Tg(DM15)26Bew View 1 model
  Tg(DMPK/tetO-EGFP/DMPK)5-313Masm View 1 model
  Tg(DMWD,DMPK*,SIX5)328Ggo View 1 model
  Tg(DMWD,DMPK*,SIX5)1177Ggo View 1 model
  Tg(HSA*LR)20aCath View 1 model
  Tg(HSA*LR)20bCath View 1 model
  Tg(HSA*LR)21Cath View 1 model
  Tg(HSA*LR)32aCath View 1 model
  Tg(HSA*LR)32bCath View 1 model
  Tg(HSA*LR)41Cath View 1 model
References Disease References using Mouse Models (23)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/08/2014
MGI 5.20
The Jackson Laboratory