Using an sgRNA and CRISPR/Cas9 technology, a FLAG sequence with a 5' GGATCC (Gly-Ser) spacer was inserted at the 3' end of the coding sequence immediately upstream of the stop codon. Donor ssDNA, sgRNA and Cas9 mRNA were injected into zygotes. (J:243766)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count