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
基因编辑小鼠
Trp53
tm1Glo
Alias:
p53
-
p53R172Hdeltag
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
为了在人类的R175H位置替换为arginine(R172H),采用了一步两步的方法。首先,通过同源重组用一个新合成的插件替换2-6号外显子。接着,使用包含2-6号外显子且在第172位密码子有CGC到CAC的错义突变的载体,替换掉新插件,重建基因。SSCP分析证实了突变基因座的整合,限制性酶切分析确认了基因的重建。用来自纯合突变胚胎的鼠胚胎成纤维细胞进行的免疫沉淀实验表明,突变蛋白的表达水平与野生型相当。RT-PCR分析检测到了完整转录本以及由于2号内含子splice接受点突变导致的3号外显子缺失的两种突变转录本。(来源:J:61683)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
2386273
129S7/SvEvBrd-Hprt1+
Targeted
Insertion, Nucleotide substitutions
--
1
65
11
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