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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
Ostm1
gl
Alias:
gl
grey lethal
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基础信息
表型特征
文献报道
灰色致命鼠的突变被确定为基因组中5'端区域的一个基因缺失。这个缺失区域长达7.5kb,包含了启动子、第一个外显子以及部分第一个内含子。基因组序列中还包括了在缺失点位处,一个LINE1线粒体重复元素的3'端序列,长度为460bp。(来源:J:82658)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
1856885
STOCK Tyrc-e
Spontaneous
Intragenic deletion, Transposon insertion
隐性
1
2
22
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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