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中文
在内含子1中插入了LoxP位点，随后在内含子2中加入了第二个LoxP位点和FRT序列，伴随着诺卡因抗性基因座。通过Cre介导的删除（Tek-cre转基因），实验确认了第2外显子的缺失，以及该等位基因的表达缺失。(来源：J:294294)
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
