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中文
Exon 2被替换为一个经过修改的版本，其中有一个点突变导致了第30位氨基酸由脯氨酸替换为苯丙氨酸(Pro30Ala)，这模拟了某些帕金森病患者中发现的突变。通过Cre介导的重组，去除了位于exon 1a和exon 1b之间的floxed Neo抗性 cassette。(来源：J:201391)
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
