Dmd^em21Gpt
Endonuclease-mediated Allele Detail

Summary

• Symbol: Dmd^em21Gpt
• Name: dystrophin, muscular dystrophy; endonuclease-mediated mutation 21, GemPharmatech
• MGI ID: MGI:7576314
• Synonyms: Dmd^em21Cd701E50
• Gene: Dmd Location: ChrX:81992476-84249747 bp, + strand Genetic Position: ChrX, 38.38 cM, cytoband C
• Alliance: Dmd^em21Gpt page

Mutation origin

• Strain of Origin: C57BL/6JGpt

Mutation description

• Allele Type: Endonuclease-mediated (Null/knockout)
• Mutation: Intragenic deletion
• CRISPR-targeting generated a null allele by deleting 701 bp from exon 21. (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)