A TI{CRIMIC.TG4.2} DNA cassette has been inserted into Cndp2, in a coding intron, and is predicted to gene trap all annotated transcripts of the gene. In addition, the coding exons of Cndp2 downstream of the inserted gene trap cassette have been deleted. The TI{CRIMIC.TG4.2} cassette was inserted via the CRISPR/Cas-9 hybrid technique, using two gRNAs that target Cndp2 : one targeted to a coding intron (TGAAACGCTCTAATCTCCTTAGG) and the other to a non-coding exon in the 3' UTR (ATGTTTACTAAACAATGTACAGG).