Human Disease	Myotonic Dystrophy 1; DM1 OMIM ID: 160900
Synonyms	Dystrophia Myotonica 1; Dystrophia Myotonica; DM; Steinert Disease
View all models	View ALL (14) 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(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