An EGFP-neo was inserted in frame 9 bp downstream of ATG. Southern blot and RT-PCR indicated recombination was successful and no wild-type transcript was present in mutant splenocytes. Flow cytometry showed lack of surface expression of the endogenous protein. GFP expression inversely correlated with the loss of Klre1 expression. (J:92262)
Basic Information
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count