A targeting vector was designed to insert a frt-flanked PGK-neo and a loxP site into intron 15 and a second loxP site into intron 19. The floxed exons encode the catalytic domains. The neo was removed via FLP mediated recombination. Western blot confirmed that this is a silent mutation. (J:107386)
Basic Information
(C57BL/6 x 129S4/SvJae)F1
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count