The loxP site flanked STOP cassette was removed from Trp53tm2Tyj via Cre-mediated recombination, allowing the expression of a p.R172H missense mutation (G>A) in exon 5. Quantitative RT-PCR confirmed that the point mutation allele is expressed at a level comparable to wild-type. (J:95316)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count