Using the CRISPRCas9 technology, donor oligos were designed to change the W562 codon TGG (W) to GCG (A) in the mouse Gm960 gene, and to introduce a silentmutation (A to G) to generate a PstI restriction site. (J:331787)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count