About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5688354
Allelic
Composition
Dmdmdx/Dmdmdx
Genetic
Background
D2.B10-Dmdmdx
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dmdmdx mutation (31 available); any Dmd mutation (154 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• Background Sensitivity: increased fat accumulation in comparison to Dmdmdx mice on the C57BL/10 background

behavior/neurological
• Background Sensitivity: mice run shorter distances than wild-type and Dmdmdx mice on the C57BL/10 background
• mice run 45% (male) and 56% (female) shorter distances than wild-type
• maximum running speed in both males and females is less than in wild-type mice

growth/size/body
• decreased body weight as compared to wild-type

homeostasis/metabolism
• Background Sensitivity: mice run shorter distances than wild-type and Dmdmdx mice on the C57BL/10 background
• mice run 45% (male) and 56% (female) shorter distances than wild-type
• maximum running speed in both males and females is less than in wild-type mice

muscle
• Background Sensitivity: weight of quadriceps femoris is less than both wild-type and Dmdmdx mice on the C57BL/10 background
• Background Sensitivity: decreased number of total myofibers in comparison to Dmdmdx mice on the C57BL/10 background
• Background Sensitivity: in comparison to Dmdmdx mice on the C57BL/10 background
• Background Sensitivity: weights of tibialis anterior and gastrocnemius muscles are less than both wild-type and Dmdmdx mice on the C57BL/10 background
• Background Sensitivity: increased fibrosis volume in quadriceps femoris as compared to Dmdmdx mice on the C57BL/10 background
• Background Sensitivity: mice exhibit lower grip strength test scores than wild-type mice and Dmdmdx mice on the C57BL/10 background

limbs/digits/tail
• Background Sensitivity: weight of quadriceps femoris is less than both wild-type and Dmdmdx mice on the C57BL/10 background

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Duchenne muscular dystrophy DOID:11723 OMIM:310200
J:160773


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory