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中文
在第六个内含子插入了loxP引导的诺姆西林插件，并在第三个loxP位点位于第三内含子。通过Cre介导的重组，去除了4到6号外显子。这种缺失导致了框架错乱的突变。蛋白表达缺失通过在脾、胸腺、肾、肝和脑的提取物中进行 Western Blot 来确认。（来源：J:153216）
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
