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Allele : Wrn<tm1Lgu> Werner syndrome RecQ like helicase; targeted mutation 1, Leonard Guarente

Primary Identifier  MGI:2386438 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Wrn
Transmission  Germline Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  The 3'-most exon encoding part of the catalytic helicase domain was replaced with a beta-geo cassette via homologous recombination. The null allele was confirmed by Western blot analysis of ear fibroblasts derived from homozygous mutant animals. No protein product was detected using antibodies directed against the N- and C-terminal regions of Wrn.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • WRN-,
  • WRN-
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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

13 Publication categories