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中文
这个来自项目Ccng2-8345J-F4819的等位基因是在Jackson实验室通过向细胞注射Cas9 RNA和4个指导序列（TGCATCTAAGAGAAGCAACA, CTGAAATGTAAAATGATTGT, GTCTGTCCAGACTTTCGACT, GCAGCCACGCTGAAGGCCTG）产生的，导致了从第五号染色体正链93,270,724bp的ATGGCATTATTTCAAGCGTC开始，到93,271,130bp后AGTCTGTCCAGACTTTCGAC位置的407bp缺失。这个变异删除了第4个外显子，并伴随着156bp的上游和下游内含子序列，包括剪接点的接受者和供体，预测会导致92号残基后的氨基酸序列改变以及随后的7个早期终止。(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
