这个来自TCPR0430项目的等位基因是在phenogenomics中心通过向细胞注射Cas9 mRNA和四条带有TCAAGAATCGACGTTCTGGC和GCTTTGATCTTCGTGCTAAC的引导RNA,目标区域的5'端是CAGATGCCCCCCAAGTCAAG,3'端是GGATCTATGAACCTCCGGCC,导致了chr6染色体从92,242,876到92,243,833的958bp缺失,1bp插入A,以及92,242,807到92,242,810的4bp删除(GRCm38)。这个变异预测会导致从第16位氨基酸开始的移码,随后的24个氨基酸发生早期截断(p.L16Qfs*26)。(J:200814)
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This allele from project TCPR0430 was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and four guide RNAs with spacer sequences of TCAAGAATCGACGTTCTGGC and GCTTTGATCTTCGTGCTAAC targeting the 5' side and CAGATGCCCCCCAAGTCAAG and GGATCTATGAACCTCCGGCC targeting the 3' side of the target region resulting in a 958-bp deletion of Chr6 from 92242876 to 92243833 with 1-bp insertion of A and a 4-bp deletion from 92242807 to 92242810 (GRCm38). This mutation is predicted to cause a frameshift with the amino acid changes after residue 16 and early truncation 24 amino acids later (p.L16Qfs*26). (J:200814)