Log In|Sign Up
中文
通过Cre介导的重组，一个包含7到9号外显子的基因片段被删除，这个片段是由上游的floxed neo cassette和下游的单个LoxP位点驱动的。 intron 6中保留了一个LoxP位点。被删除区域编码的是干扰素诱导型ADAR的707到870个氨基酸序列。(来源：J:87715, J:142338)
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
