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Phenotypes Associated with This Genotype
Genotype
MGI:3655090
Allelic
Composition
Dmdmdx/Y
Foxk1tm1Djg/Foxk1tm1Djg
Genetic
Background
involves: 129S4/SvJae * C57BL/10ScSn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdmdx mutation (42 available); any Dmd mutation (159 available)
Foxk1tm1Djg mutation (0 available); any Foxk1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die within a few weeks of birth
• few survive beyond weaning
• all are dead by 3 months of age

behavior/neurological
• fragile and weak

muscle
• fibrosis in muscles of the chest wall, the diaphragm and the intercostals

Mouse Models of Human Disease
OMIM ID Ref(s)
Muscular Dystrophy, Duchenne Type; DMD 310200 J:62225


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
09/27/2016
MGI 6.05
The Jackson Laboratory