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Allele : Raf1<tm1.1Bgn> v-raf-leukemia viral oncogene 1; targeted mutation 1.1, Benjamin G Neel

Primary Identifier  MGI:5003364 Allele Type  Targeted
Attribute String  Not Specified Gene  Raf1
Transmission  Germline Strain of Origin  (129S6/SvEvTac x C57BL/6NCrl)F1
Is Recombinase  false Is Wild Type  false
molecularNote  A floxed cDNA of exons 13 through 16 and a neo cassette were inserted upstream of exon 13. Exon 16 was replaced with one in which nucleotide substitutions result in the amino acid substitution of valine for leucine at position 613 (L613V). Cre-mediated recombination removed the cDNA and neo cassette. The amino acid substitution is a kinase activating mutation associated with Noonan syndrome.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Raf1<tm1.1Ara>,
  • Raf1<L613V>,
  • Raf1<tm1.1Ara>,
  • Raf1<L613V>
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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

10 Publication categories