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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dmdtm1Mok
targeted mutation 1, Motoya Katsuki
MGI:2429942
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dmdtm1Mok/Dmdtm1Mok involves: 129S/SvEv MGI:3722313
ot2
Dmdtm1Mok/Y involves: 129S/SvEv MGI:3722314


Genotype
MGI:3722313
hm1
Allelic
Composition
Dmdtm1Mok/Dmdtm1Mok
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdtm1Mok mutation (2 available); any Dmd mutation (153 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• in the plasma membrane of the extensor digitorum longus, caveola density is increased while the density of intramembranous particles is decreased




Genotype
MGI:3722314
ot2
Allelic
Composition
Dmdtm1Mok/Y
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdtm1Mok mutation (2 available); any Dmd mutation (153 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• at 4 and 4.5 months of age, the diaphragm exhibits an increase in connective tissue
• at 4 and 4.5 months of age, dissected muscles are whitish and hypertrophic
• several muscles exhibit an increase in size and an increase in connective tissue with necrotic fibers
• muscle degeneration is similar to that observed in other Dmd deficient mice

cellular
• in the plasma membrane of the extensor digitorum longus, caveola density is increased while the density of intramembranous particles is decreased

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Duchenne muscular dystrophy DOID:11723 OMIM:310200
J:43164





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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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory