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Dmdmdx
Spontaneous Allele Detail
Nomenclature
Symbol: Dmdmdx
Name: dystrophin, muscular dystrophy; X linked muscular dystrophy
MGI ID: MGI:1856328
Synonyms: mdx, pke, pvruvate kinase expression
Gene: Dmd  Location: ChrX:82948870-85206141 bp, + strand  Genetic Position: ChrX, 38.38 cM, cytoband C
Dmdmdx/? Myod1tm1Jae/Myod1tm1Jae mice develop cardiomyopathy

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C57BL/10ScSn
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 35 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 24 strains available      Cell Lines: 0 lines available
Carrying any Dmd Mutation:  122 strains or lines available
References
Original:  J:28684 Moore K, et al., Research News (Dmd). Mouse News Lett. 1981;64:61
All:  655 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/01/2014
MGI 5.18
The Jackson Laboratory