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Allele : Krt79<tm2b(KOMP)Wtsi> keratin 79; targeted mutation 2b, Wellcome Trust Sanger Institute

Primary Identifier  MGI:5708243 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Krt79
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  Cre-mediated excision of the parental Krt79tm2a(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.
  • mutations:
  • Intragenic deletion,
  • Insertion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

6 Publication categories