Log In|Sign Up
中文
通过同源重组，替换了一个PGK-neo cassette，导致了在exon 2的起始翻译位点被干扰，因此在来自纯合缺失胚胎的MEF中，通过免疫印迹检测不到蛋白质(来源：J:137062)
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
