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中文
携带突变人 huntington 基因(145Q)的cDNA构建，从大约aa1000处的difiglia位点被设计插入到小鼠的内源性htt基因座。由于删除了部分启动子区域和exon1，内源性htt基因的表达被干扰了。(来源：J:147112)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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
