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Allele : Ptpn11<tm4.2Bgn> protein tyrosine phosphatase, non-receptor type 11; targeted mutation 4.2, Benjamin G Neel

Primary Identifier  MGI:5004658 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Ptpn11
Transmission  Germline Strain of Origin  129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
molecularNote  A loxP site was inserted upstream of exon 7. An inverted modified exon 7 with a nucleotide substitutions that result in the amino acid substitution of cysteine for tyrosine at position 279 (Y279C) with a 5' loxP site was flanked by loxP511 sites and inserted downstream of exon 7 along with an FRT flanked neo cassette. Flp-mediated recombination removed the neo cassette, and cre-mediated recombination removed the endogenous exon 7 and reverted the orientation of the modified exon 7. The amino acid substitution is one of the two most common mutations in Leopard syndrome.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Ptpn11<Y279C>,
  • Ptpn11<Y279C>,
  • Ptpn11<LS>,
  • Ptpn11<LS>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

12 Publication categories