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Allele : Dsg2<tm1d(EUCOMM)Wtsi> desmoglein 2; targeted mutation 1d, Wellcome Trust Sanger Institute

Primary Identifier  MGI:6501716 Allele Type  Targeted
Attribute String  Null/knockout Gene  Dsg2
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
molecularNote  The L1L2_Bact_P cassette was inserted at position 20711672 of Chromosome 18 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon(s) at position 20712812. The critical exons 4 and 5 are thus flanked by loxP sites. Flp-mediated recombination removed the lacZ and neomycin resistance gene and subsequent cre expression deleted exons 4 and 5. Exon 4 and 5 deletion causes a frameshift mutation and premature termination of translation.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Dsg2<mut>,
  • Dsg2<mut>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

7 Publication categories

Trail: Allele