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中文
CRISPR/cas9基因编辑产生了一个1个碱基的插入，紧随其后是一个3个碱基的删除（插入/缺失突变）。这个净2个碱基的删除预计会导致Cys-286位置的框架移位，影响71个氨基酸，并在3' UTR内的TAA终止密码子处停止。(来源：J:94077)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
