Log In|Sign Up
中文
在exon 1的上游和内含子1位置插入了LoxP位点，形成了一个可调控的等位基因，exon 1被敲除了。exon 1包含起始翻译位点，其缺失会导致无功能的突变体。同时，内含子1中插入的带有FRT序列的抗氨苄青霉素基因座通过Flp介导的重组被去除了。（来源：J:241413）
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
