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Allele : Wrn<tm1Led> Werner syndrome RecQ like helicase; targeted mutation 1, Philip Leder
Primary Identifier  MGI:2156622 Allele Type  Targeted
Attribute String  Null/knockout Gene  Wrn
Transmission  Germline Strain of Origin  129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
molecularNote  Exons 3 and 4 were replaced with a neomycin selection cassette. The targeted allele is expected to express a fully translated protein that lacks 121 amino acids of the helicase domain.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Wrn<deltahel>,
  • Wrn<deltahel>,
  • WS,
  • WS
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

20 Publication categories

Trail: Allele




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