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中文
在2号和3号外显子周围插入了LoxP位点和一个由FRT引导的诺卡因选择子。通过Flp介导的重组移除了选择子。在生殖细胞中，Cre介导的重组导致了2号和3号外显子以及诺卡因选择子的缺失。北半球分析证实了成年纯合突变肾中mRNA表达的缺失。(来源：J:258919)
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
