A targeting vector was designed such that the codons of the five C-terminal amino acids, VWRPY, were changed to the stop codon UAG and to codons encoding substituted amino acids designed to create a new NotI site. A loxP-flanked neo was included in intron 5 and was subsequently removed via cre-mediated excision. RT-PCR and Western blot analyses demonstrated expression of the mutant transcript and protein, respectively. (J:109584)
Basic Information
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Insertion, Nucleotide substitutions
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count