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Allele : Braf<tm1Cpri> Braf transforming gene; targeted mutation 1, Catrin Pritchard

Primary Identifier  MGI:3612533 Allele Type  Targeted
Attribute String  Conditional ready, Humanized sequence, No functional change Gene  Braf
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  A targeting vector was designed to insert an ENSMUST00000002487:c.1910T>A mutation (leading to a p.V637E substitution) into exon 18 (ENSMUST00000101497 exon 15). A loxP site, a minigene (cDNA sequence encoding exons 15-18 (last exon) of wild-type Braf splice variant ENSMUST00000101497 with alpha-globin splice acceptor sequences at the 5' end and alpha-globin pol(A) signal sequences at the 3' end), and a loxP site flanked neomycin resistance gene cassette were inserted into intron 17. Upon cre expression, the minigene-STOP-neo cassette is deleted, enabling expression of the mutated sequence. This mutation increases the kinase activity of the protein and is the equivalent of the human c.1799T>A (p.V600E) mutation, the most common oncogenic mutation in BRAF.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • LSL-B-raf<V600E>,
  • LSL-BRAFV600E,
  • LSL-BRAFV600E,
  • LSL-B-raf<V600E>,
  • V600E,
  • V600E
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

57 Publication categories