Log In|Sign Up
中文
在内含子1插入了一个frt和loxP修饰的neo cassette，通过同源重组在内含子2中插入了第三个loxP位点。通过Cre介导的重组，neo cassette和exon 2被去除。exon 2的缺失导致了ATg启动子的丧失。在囊胚中，蛋白表达的缺失得到了确认。(来源：J:145744)
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
