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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
Vhl
tm1.1Whkr
Alias:
Vhl
M1L
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基础信息
表型特征
文献报道
在第1外显子被替换为一个修改过的第1外显子,其中由ATG替换为CTA的核苷酸变异导致第1位氨基酸由甲硫氨酸变为亮氨酸(即p.Met1Leu)。这个突变阻止了长型isoform的表达。通过Cre介导的重组,去除了位于修改第1外显子下游的Neomycin抗性基因簇。 Western blot结果显示肾和肝中未检测到长型isoform的表达,而短型isoform的表达有所增加。(来源:J:198361)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
5529337
129
Targeted
Insertion, Nucleotide substitutions
--
1
11
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
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