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中文
在exon 2的上游插入了一个loxP位点。随后插入了一个带有FRT标签的诺卡因抗性元件和另一个loxP位点在exon 3的下游。通过Flp介导的重组去除了选择性元件，使得exons 2和3成为可删除的。通过Cre介导的重组，移除了exons 2和3，产生了缺失N端的截短蛋白。(来源：J:233694)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
