Log In|Sign Up
中文
在exon 5的上游插入了loxP位点。在exon 6之后插入了一个带有3' loxP的FRT引导的诺卡因抗性基因座，其中也包含了一个loxP位点。通过Cre介导，5和6号外显子以及选择性基因座一起被去除。蛋白表达缺失通过在小鼠胚胎成纤维细胞中进行 Western blot 分析得到了确认。(来源：J:262629)
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
