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Dmdem2Gpt
Endonuclease-mediated Allele Detail
Summary
Symbol: Dmdem2Gpt
Name: dystrophin, muscular dystrophy; endonuclease-mediated mutation 2, GemPharmatech Co., Ltd
MGI ID: MGI:7462097
Synonyms: Dmdem1Cin(C3197T)
Gene: Dmd  Location: ChrX:81992476-84249747 bp, + strand  Genetic Position: ChrX, 38.38 cM, cytoband C
Alliance: Dmdem2Gpt page
Mutation
origin
Strain of Origin:  C57BL/10ScSnJGpt
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Insertion
 
Mutation detailsCRISPR-targeting introduced the mutation responsible for the amino acid substitution of cysteine for threonine at position 3197 (C3197T). (J:293217)
Inheritance:    Not Specified
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:  167 strains or lines available
References
Original:  J:293217 GemPharmatech, GemPharmatech Website. 2020;
All:  1 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
01/20/2026
MGI 6.24
The Jackson Laboratory