Exons 6-10 were replaced with a construct containing exons 6 and 7, a loxP site, a minigene containing exons 8-11, a polyadenylation STOP sequence, a FRT-flanked neomycin resistance gene, a second loxP site, a mutated exon 8, and exons 9-10. The mutated exon 8 contains a C to T mutation at position 1402 and a G to T mutation at position 1404, resulting in an arginine to cysteine change at amino acid 468. The R468C mutation corresponds to the human R465C mutation, frequently detected in primary tumors. The mutant is expressed only after cre-mediated recombination. (J:258194)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6NSlc
Targeted
Insertion, Nucleotide substitutions
--
1
2
1

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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