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Allele : Prss8<tm1.1Bug> serine protease 8 (prostasin); targeted mutation 1.1, Thomas H Bugge

Primary Identifier  MGI:5588579 Allele Type  Targeted
Attribute String  Not Specified Gene  Prss8
Transmission  Germline Strain of Origin  129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
molecularNote  A T to G nucleotide substitution was introduced into exon 6 at nucleotide 943 by homologous recombination. This point mutation causes the substitution of the active site serine 238 within the catalytic histidine-aspartate-serine triad with alanine (S238A) and renders it catalytically inactive. In addition, a loxP flanked neomycin cassette under the control of the 3-phosphoglycerate kinase promoter was inserted upstream of the substitution. The neomycin cassette was removed via Cre-mediated recombination by mating with Tg(EIIa-cre)C5379Lmgd transgenic mice. RT-PCR indicates that the introduction of the point mutation and the loxP site in intron 5 do not affect mRNA expression. Western blot analysis shows that protein is expressed at levels similar to wild-type and the presence of a faster migrating species in the kidney and lung.
  • mutations:
  • Insertion,
  • Single point mutation
  • synonyms:
  • Prss8<Cat->,
  • Prss8<Cat->
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

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0 Driven By

6 Publication categories

Trail: Allele