About Help FAQ

Symbol
Name
ID

Dmd
dystrophin, muscular dystrophy
MGI:94909

Phenotype annotations related to behavior/neurological

*	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	Fatigue	Myalgia
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

Dmd^{em1(IMPC)Hmgu}/Dmd^{em1(IMPC)Hmgu}

Dmd^em4Eno/Dmd^em4Eno

Dmd^mdx/Dmd^mdx

!

!

Dmd^em1Eno/Y

Dmd^em4Eno/Y

Dmd^mdx-3Cv/Y

Dmd^mdx-4Cv/Y

Dmd^mdx-5Cv/Y

Dmd^mdx/Y

*

Dmd^tm1Kmf/Y

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 04/16/2024 MGI 6.23