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中文
CRISPR/Cas9基因编辑引入了chr7:29013738到29013752位置的16bp缺失，这是在基因96的外显子区域。测序N1后代后发现，修复模板没有整合到这个等位基因中，这是由于非同源末端连接修复造成了双链断裂。来源：J:275500
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
