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Dmdmdx-4Cv
Chemically induced Allele Detail
Nomenclature
Symbol: Dmdmdx-4Cv
Name: dystrophin, muscular dystrophy; X linked muscular dystrophy 4, Verne Chapman
MGI ID: MGI:1856331
Synonyms: mdx4cv, mdx4cv, mdx4cv, mdxCv4
Gene: Dmd  Location: ChrX:82948870-85206141 bp, + strand  Genetic Position: ChrX, 38.38 cM, cytoband C
Mutation
origin
Strain of Origin:  C3Ha.Cg-Hprta Pgk1a
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
    A C to T transition in exon 53 at position 7916 creates a premature stop codon. (J:34517)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 33 assay results
In Structures Affected by this Mutation: 2 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Dmd Mutation:  152 strains or lines available
References
Original:  J:9638 Chapman VM, et al., Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice. Proc Natl Acad Sci U S A. 1989 Feb;86(4):1292-6
All:  46 reference(s)

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)
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last database update
01/21/2020
MGI 6.14
The Jackson Laboratory