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使用CRISPR/Cas9系统和sgRNA5'-TGCACTCGCGGACCCTGTCG-3'产生了这些小鼠。CRISPR/Cas9系统在c.231_232位点产生了一个2个碱基的缺失（NM_029098.3）。预测的变异会导致蛋白质产品从第17个氨基酸开始出现框架移位，并在额外插入30个异常氨基酸后过早终止。(来源：J:274568)
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
