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中文
在前导序列上游插入了loxP位点，接着在内含子1中插入了FRT表型开关位点和诺卡因抗性基因座，再配对一个loxP位点。通过RT-PCR分析，发现诺卡因基因座干扰了该等位基因的转录。随后通过flp介导的重组去除了诺卡因基因座。接着，通过cre介导的重组删除了exon 1，形成了无功能的等位基因。RT-PCR确认了这个等位基因转录本的减少。(来源：J:239934)
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
