Krt79^{tm2b(KOMP)Wtsi}
Targeted Allele Detail

Summary

• Symbol: Krt79^{tm2b(KOMP)Wtsi}
• Name: keratin 79; targeted mutation 2b, Wellcome Trust Sanger Institute
• MGI ID: MGI:5708243
• Gene: Krt79 Location: Chr15:101837767-101848759 bp, - strand Genetic Position: Chr15, 57.14 cM
• Alliance: Krt79^{tm2b(KOMP)Wtsi} page
• IMPC: Krt79 gene page

Mutation origin

• Mutant Cell Line: EPD0179_4_A12
• Germline Transmission: Earliest citation of germline transmission: J:204739
• Parent Cell Line: JM8.N4 (ES Cell)
• Strain of Origin: C57BL/6N
• Project Collection: KOMP-CSD

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_Bact_P
• Mutation details: Cre-mediated excision of the parental Krt79^{tm2a(KOMP)Wtsi} allele resulted in the removal of the promoter-driven neomycin selection cassette and critical exon(s) leaving behind the inserted lacZ reporter sequence. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml. (J:204739)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Krt79 Mutation: 37 strains or lines available

References

• Original: J:204739 International Knockout Mouse Consortium, MGI download of modified allele data from IKMC and creation of new knockout alleles. Database Download. 2014-2023
• All: 4 reference(s)