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中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和指导序列AATGGCATTGGTGACAGGCG和ATTTGACCATTACCACCTAA产生的，导致了18号染色体60,579,121到60,579,739位置的619bp缺失。这个变异删除了基因ENSMUSE00000355110（第4和5外显子）以及429bp的内含子序列，包括剪接点的接受者和捐赠者，预测会导致从第72位氨基酸后发生序列改变，并在接下来的5个位置发生早期截断。(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
