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
Oprm1
tm2.1Shlz
Alias:
MOR
10S/T-A
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
在exon 3b的位置替换了一段,其中的核苷酸变异导致了 alanine 替换为 serine 或 threonine:T354A(AC到GCC)、S355A(TCC到GCC)、S356A(TCC到GCC);T357A(ACA到GCA)、S363A(TCT到GCC)、T370A(AC到GCC)、S375A(TCC到GCC)、T376A(ACG到GCC)、T379A(ACA到GCA)、T383A(AC到GCC)。通过Cre介导,去除了在修改后的exon 3b下游插入的neo抗药性 cassette。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
6117668
C57BL/6
Targeted
Insertion, Nucleotide substitutions
--
1
--
1
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