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中文
CRISPR/cas9导向的基因组编辑用于在c.3583-9位点创建一个G到A的单个碱基替换，这会形成一个隐蔽的剪接接受位点和提前终止密码子在第16个内含子。异常的剪接导致mRNA转录本中插入了7个碱基。该变异通过测序和Southern blot方法进行了确认。(来源：J:341855)
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
