Log In|Sign Up
中文
Exon 2被替换成一个带有floxed Neo抗性标记、终止子、LoxP位点、去除了N端编码序列的人源ETV1cDNA（包括内含子和GFP以及polyA序列），通过Cre介导的重组，移除了选择和终止子元件，从而实现了融合产物和报告基因的表达。（来源：J:212219）
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
