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Human Disease and Mouse Model Detail
Human Disease Myopathy, Myofibrillar, 1; MFM1
OMIM ID: 601419
Synonyms Arrhythmogenic Right Ventricular Cardiomyopathy 7, Formerly; ARVC7, FORMERLY; Arrhythmogenic Right Ventricular Dysplasia, Familial, 7, Formerly; ARVD7, FORMERLY; Cardiomyopathy, Dilated, 1f and Limb-Girdle Muscular Dystrophy Type 1d, Formerly; Cardiomyopathy, Dilated, with Conduction Defect and Muscular Dystrophy; CDCD3, FORMERLY; Cmd1f and Lgmd1d, Formerly; Desmin-Related Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy; Desmin-Related Myopathy; DRM; Desminopathy, Primary; Inclusion Body Myopathy 1, Autosomal Dominant, Formerly; IBM1, FORMERLY; Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy; Myopathy, Myofibrillar, Desmin-Related
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

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Des* DES* View 1 model 1:1 Homology
     Ldb3* View 1 model 1:0 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
06/05/2013
MGI 5.13 		The Jackson Laboratory