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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TCTAGGATCAGTAATTGCCA和AGTTCAAACATCCCTACAAA产生，导致了1328bp的缺失，起始于161,031,517bp的染色体1位置，直到161,032,844bp后。这个变异删除了ENSMUSE00000947438（第3外显子）以及368bp的上下游内含子序列，包括剪接接受点和捐赠点，预测会形成一个无功能的等位基因。（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
