A superfolder GFP (sfGFP) coding sequence followed by a flexible linker spacer sequence (GSGSGS) has been inserted into the endogenous Lgr3 locus at the N-terminal end of the Lgr3 open reading frame. The Lgr3 open reading frame contains a 1bp deletion in the Lgr3 sequence just downstream of the site of the insertion, resulting in a premature termination codon.
CRISPR/Cas9 knock-in mutation is a 1 bp deletion in the tagged Lgr3 coding sequence, resulting in early translation termination.