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中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列(TCTACACTGCAAAGAGAGCA, ACTTACTACCTCTCTAGAAC)产生的，导致了119,702,388到119,702,935bp的157bp染色体13上的缺失。这个变异删除了ENSMUSE00001063943(第5外显子)以及382bp的内含子序列，包括剪接点和起始点，预测会导致246号残基后的氨基酸序列改变以及随后的4个氨基酸的早期截断。(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
