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Phenotypes Associated with This Genotype
Genotype
MGI:6507848
Allelic
Composition		 Dmdmdx/Y
Tg(DMD*)#Spc/0
Genetic
Background		 involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdmdx mutation (30 available); any Dmd mutation (153 available)
Tg(DMD*)#Spc mutation (1 available); any Tg(DMD*)#Spc mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
muscle
myositis ( J:280218 )
• muscle inflammation
skeletal muscle fibrosis ( J:280218 )
• muscle shows features of fibrosis

immune system
myositis ( J:280218 )
• muscle inflammation

homeostasis/metabolism
abnormal calcium level ( J:280218 )
• muscle shows calcium deposits

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
Duchenne muscular dystrophy DOID:11723 OMIM:310200
 J:280218

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory