Symbol Name ID |
Dmd
dystrophin, muscular dystrophy MGI:94909 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Fatigue |
Myalgia |
Disease(s) Associated with DMD | ||
Becker muscular dystrophy |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal motor capabilities/coordination/movement |
tremors |
impaired coordination |
abnormal grip strength |
decreased grip strength |
abnormal gait |
short stride length |
fatigue |
impaired exercise endurance |
decreased aerobic running capacity |
|
Availability | Mouse Genotype | |||||||||||
Dmdem1(IMPC)Hmgu/Dmdem1(IMPC)Hmgu | ||||||||||||
Dmdem4Eno/Dmdem4Eno | ||||||||||||
Dmdmdx/Dmdmdx | ! | ! | ||||||||||
Dmdem1Eno/Y | ||||||||||||
Dmdem4Eno/Y | ||||||||||||
Dmdmdx-3Cv/Y | ||||||||||||
Dmdmdx-4Cv/Y | ||||||||||||
Dmdmdx-5Cv/Y | ||||||||||||
Dmdmdx/Y | * | |||||||||||
Dmdtm1Kmf/Y |
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 05/14/2024 MGI 6.23 |
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