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中文
这个转基因载体包含4.8千碱基的猪酪氨酸羟化酶(Th)启动子序列，一段携带C88G突变的人类α-synuclein(SNCA)基因编码区，该突变导致阿尔法30 Pro氨基酸替换，以及SV40的polyadenylation序列。(来源：J:70209)
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
