Log In|Sign Up
中文
通过Cre介导的重组，目标敲除-先期准备-父本基因型Esys1tm1Tmss去除了3到7号的neo和creitical外显子，导致在基因的第2 intron内插入了FRT接点、splice接受器、lacZ序列以及polyadenylation序列，最后跟着一个loxP位点。(来源：J:236096)
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
