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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CGCAAGCCAGACAGCGATGC和ATGGGTCGCTCTCGGCGGAC产生的，导致了从染色体4的134,245,317bp位置开始，到134,245,493bp位置的177bp缺失。这个变异删除了ENSMUSE00000389670(第1外显子)的177bp，预测会导致从第3位氨基酸开始的序列缺失59个氨基酸，并重新进入阅读框。(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
