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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
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中文
基因编辑小鼠
Kcne1
tm1Rdn
Alias:
minK-lacZ
minK
-
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基础信息
表型特征
文献报道
整个编码区域,位于exon 2内,被替换为一个NLS-lacZ-pA PGK-neo的插入片段。在RNA酶保护实验中,对突变动物的mRNA缺失进行了确认,且在突变小鼠心肌中检测到了β-半乳糖苷酶的表达,仅限于某些区域。(来源:J:53735)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
3040614
129S6/SvEvTac
Targeted
插入,基因内删除
--
1
7
9
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:
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Phenotypes
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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