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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ACAACTTCTTCCCAAACTAC和CCAACTGCCAAAGAGTCTAC产生的，导致X染色体56,913,220到56,919,032bp位置的5813bp缺失。这个变异删除了ENSMUSE00000386381(第3外显子)的5813bp，并预测会导致254位点后的氨基酸序列改变以及随后的9个早期终止密码子。缺失位点有一个1bp的插入(G)。(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
