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中文
在exon 2的上游插入了loxP位点，接着是带有FRT标签的诺卡因选择座和另一个loxP位点，它们位于exon 2下游。通过Flp介导的重组，删除了选择座。exon 2通过Cre介导的重组被去除。exon 2的缺失消除了Cnksr2的两种形式。(来源：J:339544)
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
