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中文
携带突变人类 Huntington 基因(145Q)在第586位氨基酸(由casp6位点剪切)被截短的cDNA构建，通过CMV早期增强子/鸡β-actin启动子的控制，被定向插入Gt(ROSA)26Sor位点，这项操作通过RMCE技术实现。(来源：J:147112, J:243843)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
