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Human Disease and Mouse Model Detail
Human Disease Myotonic Dystrophy 1; DM1
OMIM ID: 160900
Human Phenotype Ontology associations
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     DMPK* Dmpk* View 8 models HomoloGene and HGNC
     MBNL1 Mbnl1* View 1 model 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(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
  Tg(tetO-CUGBP1)3413Coop View 1 model
References Disease References using Mouse Models (28)

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