Home
Toolbox
Resource
Workflow
Tutorials
Citations
Downloads
Mutation Al-Predictor Flow
Gene-to-Mutation Flow
News & Insights
Genetic Encyclopedia
Frontiers
Industry Insights
Case Studies
About Us
About the Site
Contact Us
Private Policy
User Agreement
COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
Log In
|
Sign Up
中文
转基因模型
Tg(Tyr-cre/ERT2)1Lru
Alias:
Tyr::Cre-ERT2
Tg(Tyr-cre/ERT2)1Laru
Tyr::CreER
T2-Lar
Need animal model construction services?
Click here >>
Create a favorites folder
Cancel
Confirm
Add To Favorites
Select a favorites
Description
New favorites >>
Cancel
Confirm
Favorite
基础信息
表型特征
文献报道
这个转基因表达的是由酪氨酸酶增强子和启动子驱动的曲妥昔芬诱导型Cre重组酶,只在黑素细胞和黑素前体细胞中活性。转基因插入在7号染色体的近端,与2号染色体近端的约300万个碱基对的重复序列融合。这个插入还导致7号染色体部分区域的缺失,具体发生在Nlrp12基因的第10外显子(3,220,560,mm10小鼠基因组),包括Speer9-ps1和Au018091等centromeric序列,以及Nlrp12基因剩余的3'序列。融合到7号染色体上的2号染色体重复序列包含了Fam171a1、Nmt2、Rpp38、Olah1、Meig1和Dclre1c等基因,以及Suv39h2基因缺失1-2个外显子的部分。因此,携带Tg(Tyr-cre/ERT2)1Lru基因的动物只有一条功能正常的7号染色体,而7号染色体的基因有三条重复的2号染色体拷贝。(引用文献:J:105276, J:282623)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
3617509
C57BL/6 x DBA/2
--
Duplication, Insertion, Intergenic deletion
--
--
--
31
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
No Data Found!
微信
信息比对
科研助手
使用教程
回到顶部