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中文
在转暂时的Cre介导重组后，删除了floxed exon 2和neo cassette，留下一个loxP位点。删除exon 2理论上产生了无义突变，因为阻止了F box的编码，并在编码5个氨基酸和39个氨基酸后产生了一个错位和早停密码子。PCR确认了重组。(来源：J:89060)
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 |
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References Literature
Title
PMID
Journal
Year
IF
