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中文
Exon 2被LoxP位点前后标记，通过同源重组，插入了一个FRT-介导的neo cassette在第一个LoxP位点上游。通过Flp介导的重组移除了选择性 cassette。随后，Cre介导的重组去除了Exon 2，导致了框架移位突变。（来源：J:264147）
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
