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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GCCCCAACTGATTGTTCAAA和GGTCTGATATGCACAGACAC产生的，导致X染色体120,399,472到120,401,879bp位置的2408bp缺失。这个变异删除了ENSMUSE00000435881(第3外显子)的2408bp，并预测会导致203号残基后氨基酸序列改变以及随后的51个氨基酸早期截断。(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
