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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
Atp7a
Mo-br
Alias:
Br
Mo
br
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基础信息
表型特征
文献报道
在斑马鼠中观察到了两个显著的核苷酸变化。第11外显子中的一个6bp内含子缺失,移除了编码蛋白质中的一个Leucine(801位点)和一个Alanine(802位点,或者根据剪接变异可能为800和801),但不影响其功能的区域。此外,检测到一个G变A的突变,位于第514(或513)位点,将Alanine转换为Threonine,这个改变位于可能影响铜转运功能的区域。 Western blot分析显示,这个等位基因产生了与野生型相当水平的正常大小蛋白质。(来源:J:38978, J:41388)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
1856098
C57BL
Spontaneous
Intragenic deletion, Single point
半显性
1
4
50
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
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