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中文
这个Adad2-5594J-B项目中的等位基因是在Jackson实验室通过将Cas9 RNA和引导序列CCCATGCTCAGCGGTCCTAG注入产生的，导致了8个碱基的缺失（CTAGGACC）以及4个碱基的插入（ATGA），发生于8号染色体正链位置119,612,902bp（GRCm38），预测会导致frameshift突变和早期截断。 (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
