Wrn^em21Gpt
Endonuclease-mediated Allele Detail

Summary

• Symbol: Wrn^em21Gpt
• Name: Werner syndrome RecQ like helicase; endonuclease-mediated mutation 21, GemPharmatech Co., Ltd
• MGI ID: MGI:7308663
• Synonyms: Wrn^em21Cd20448
• Gene: Wrn Location: Chr8:33724412-33875555 bp, - strand Genetic Position: Chr8, 20.3 cM, cytoband A4
• Alliance: Wrn^em21Gpt page

Mutation origin

• Strain of Origin: C57BL/6JGpt

Mutation description

• Allele Type: Endonuclease-mediated (Null/knockout)
• Mutation: Intragenic deletion
• CRISPR-targeting introduced a coding region modification (del20448). (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 Wrn Mutation: 93 strains or lines available

References

• Original: J:293217 GemPharmatech, GemPharmatech Website. 2020
• All: 1 reference(s)