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Allele : Sox9<tm1.1Ksec> SRY (sex determining region Y)-box 9; targeted mutation 1.1, Kathryn S E Cheah

Primary Identifier  MGI:7451055 Allele Type  Targeted
Attribute String  Conditional ready, Humanized sequence, Reporter Gene  Sox9
Transmission  Germline Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  LoxP sites were inserted into intron 2 and downstream of final exon 3, and a copy of exon 3 (with a C-to-G tyrosine (TAC) to stop codon (TAG) mutation in codon 440 (p.YY440*) and with IRES sequence, the EGFP reporter gene and poly(A) signal sequences in the 3' UTR) and an FRT site flanked neomycin resistance gene cassette were inserted downstream of the gene. The neo cassette was removed through subsequent Flp-mediated recombination. This allele will express the wild-type gene only, unless conditional Cre-mediated recombination removes the endogenous exon 3, in which case the mutant exon 3 (with its premature stop codon) is expressed together with the EGFP reporter. The mutation mimics the same human mutation, which is associated with campomelic dysplasia.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Sox9<fY440X>,
  • Sox9<floxed-Y440X>,
  • Sox9<fY440X>,
  • Sox9<floxed-Y440X>
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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

5 Publication categories

Trail: Allele