The targeting construct contains the mCherry reporter open reading frame with a WPRE and the 10 target sequences (see below) inserted into the 3 UTR driven by a CAG promoter and inserted into the Igs7 locus using CRISPR/cas9 genome editing. A "barcode" 276 bp array containing 10 target sites in a unique arrangement is inserted upstream of the EGFP polyadenylation site. (J:341616)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count