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Allele : Fgfr2<tm4.1Sor> fibroblast growth factor receptor 2; targeted mutation 4.1, Philippe Soriano

Primary Identifier  MGI:6477570 Allele Type  Targeted
Gene  Fgfr2 Transmission  Germline
Strain of Origin  129S4/SvJaeSor Is Recombinase  false
Is Wild Type  false
molecularNote  Site-directed mutagenesis was used to insert nucleotide substitutions in exon 11 of the locus, altering tyrosine to phenylalanine at codon 485 (Y485F-TAT to TTT) and a silent mutation, leucine to leucine at codon 487 (L487L -TTG to CTC) and introducing a Sac1 site. The substitutions were initially described as Y466F and L468L, respectively. In addition, a loxP and FRT-flanked neomycin-resistance gene was located downstream of exon 11. Flp-mediated recombination removed the FRT-flanked neo cassette.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Fgfr2<C>,
  • Fgfr2<C>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

3 Publication categories