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中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和两个指导序列(ATACTTTCACACAAACCG, GAGACCAAACCAGCAGCATA)产生的，导致了从染色体2的32,905,645bp开始，到32,906,270bp之后的626bp区域的缺失。这个变异删除了ENSMUSE00000388163(第2外显子)以及495bp的内含子序列，包括剪接点的接受者和捐赠者，预测会导致第18位氨基酸之后序列改变以及随后的4个氨基酸早期终止。(来源：J:188991)
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
