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中文
在PR域下游插入了一个FRT-和loxP引导的诺姆霉素抗性基因座，接着在第3外显子下游插入了另一个loxP位点。通过Flp介导的重组去除了选择性基因座，随后通过Cre介导的重组剔除了第3外显子。这个PR域后的缺失导致了框架突变，从而阻止了功能蛋白的产生。(来源：J:209773)
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
