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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
Septin12
em1Haiy
Alias:
Sept12
G169E
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基础信息
表型特征
文献报道
通过CRISPR/Cas9技术,使用sgRNA和ssODN模板引物,创造了一个带有GC替换为AG的等位基因,导致编码肽的p.G167E替换(在人类同源蛋白中等同于p.G169E,来源:J:279291)。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
6363494
(FVB/NJ x B6(Cg)-Tyrc-2J/J)F1
Endonuclease-mediated
核苷酸替换
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1
2
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:
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Phenotypes
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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