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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
Mchr1
tm1Sqn
Alias:
Mchr1 KO
Mch1r
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基础信息
表型特征
文献报道
这个基因通过将第2外显子替换为诺卡因抗性载体而发生了突变。目标突变导致从第一跨膜域到终止密码子的序列缺失。通过对冠状大脑切片的原位杂交分析,证实了纯合突变动物中基因表达的缺失。(来源:J:81787)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
2451034
129S7/SvEvBrd-Hprt1b-m2
Targeted
插入,基因内删除
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1
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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:
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Phenotypes
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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