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Human Disease and Mouse Model Detail
Human Disease Facioscapulohumeral Muscular Dystrophy 1; FSHD1
OMIM ID: 158900
Synonyms Facioscapulohumeral Muscular Dystrophy; FSHD; FMD; Muscular Dystrophy, Facioscapulohumeral, Type 1; Muscular Dystrophy, Facioscapulohumeral, Type 1A; FSHD1A
View all models View ALL (3) 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
     Large* LARGE View 1 model 1:1 Homology
     DUX4*, DUX2, DUX4L2, DUX4L3, DUX4L4, DUX4L5, DUX4L6, DUX4L7   0:8 Homology
Frg1 FRG1*   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(ACTA1-Frg1)highRotu View 1 model
  Tg(ACTA1-Frg1)medRotu View 1 model
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
05/08/2013
MGI 5.13 		The Jackson Laboratory