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Dmdem1Kxi
Endonuclease-mediated Allele Detail
Summary
Symbol: Dmdem1Kxi
Name: dystrophin, muscular dystrophy; endonuclease-mediated mutation 1, Kyoko Itoh
MGI ID: MGI:7716702
Gene: Dmd  Location: ChrX:81992476-84249747 bp, + strand  Genetic Position: ChrX, 38.38 cM, cytoband C
Alliance: Dmdem1Kxi page
Mutation
origin
Strain of Origin:  (C57BL/6 x DBA/2)F1
Mutation
description
Allele Type:    Endonuclease-mediated (Epitope tag)
Mutation:    Insertion
 
Mutation details: 

CRISPR/Cas9 technology inserted an HA-tag at the Dp71-specific translation initiation site which is present in intron 62 to fuse with the N-terminal amino acid sequence of Dp71 in-frame. This tag allows for the specific detection of the short dystrophin product, Dp71, expression. (J:352582)

Expression
In Mice Carrying this Mutation: 201 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Dmd Mutation:  162 strains or lines available
References
Original:  J:352582 Fujimoto T, et al., Generation of dystrophin short product-specific tag-insertion mouse: distinct Dp71 glycoprotein complexes at inhibitory postsynapse and glia limitans. Cell Mol Life Sci. 2022 Jan 30;79(2):109
All:  2 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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Funding Information
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last database update
10/13/2026
MGI 6.29
The Jackson Laboratory