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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
Pde6b
rd1
Alias:
rodless retina
rd-1
Pdeb
rd1
rd
rd1
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基础信息
表型特征
文献报道
在rd1小鼠中已经识别到两种突变。一种是Xmv-28小鼠白血病病毒(reverse orientation in intron 1)的插入,这种插入存在于所有具有rd1表型的鼠种中。另外,所有rd1小鼠的基因型中都存在一个导致蛋白质部分缺失的致病突变,即第347位的密码子由C变为A的转换,这导致了编码蛋白的截断,包括催化区域。这种突变转录本在前体mRNA剪接过程的前后都有特定的降解机制(来源:J:4366, J:11513, J:51361)。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
1856373
various
Spontaneous
Single point , Viral insertion
隐性
1
8
432
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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