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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(GAGACCCGAGCCTGGAGAAG, CCCCGCGCGCGGGACAGCGG)产生的，导致了7号染色体99,625,502到99,626,632bp位置的1131bp缺失。这个变异删除了ENSMUSE00001008045(第1外显子)的1131bp，预测会导致从第4位氨基酸开始的序列改变，删除378个氨基酸，然后在终止密码子前的两个氨基酸重新回到阅读框内。(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
