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中文
从exon 1的最后6个核苷酸和intron 1的前51个核苷酸替换成一个能诱导的cre重组酶基因，连接着一个改良的雌激素受体(ERT2)、一个loxP位点和一个FRT标记的诺卡因抗性基因。通过Flp介导的重组，去除了选择性基因座。(来源：J:217599)
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
