Symbol Name ID |
Dmd
dystrophin, muscular dystrophy MGI:94909 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Difficulty walking |
Intellectual disability, mild |
Obstructive sleep apnea |
Hyporeflexia |
Falls |
Loss of ambulation |
Tip-toe gait |
Waddling gait |
Delayed gross motor development |
Disease(s) Associated with DMD | |||||||||
Becker muscular dystrophy | |||||||||
Duchenne muscular dystrophy |
Mouse Phenotypes | nervous system phenotype |
abnormal corticotroph morphology |
increased somatotroph cell size |
abnormal Muller cell morphology |
abnormal neuromuscular synapse morphology |
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Availability | Mouse Genotype | |||||
Dmdmdx-3Cv/Dmdmdx-3Cv | ||||||
Dmdmdx/Dmdmdx | * | |||||
Dmdmdx-3Cv/Y | ||||||
Dmdmdx/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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