The allele was generated by introducing a cassette containing a CreERT2 upstream of IRES-nlacZ followed by a FRT-flanked neo cassette (CreERT2-IRES-nLacZ-FRT-neo-FRT) into the ATG translational site in exon 3 of the Prdm1 gene via homologous recombination in embryonic stem (ES) cells. Correctly targeted ES cell clones were transiently transfected with a FLP expression construct to excise the neo cassette. (J:257197)
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cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count