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中文
CRISPR/Cas9在C57BL/6J纯系背景上的Sema6a基因修饰，产生了20个碱基对编码序列的缺失，目标区域在特定外显子。预测会导致密码子框架移位和下游下一个外显子的过早终止。(来源：J:338850)
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
