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中文
基因组序列从exon 1到exon 3的部分被替换为：5'端的loxP位点、lacZ基因、frt标记的neo cassette、再次的loxP位点以及polyadenylation序列。通过脑组织的 Western blot 分析，证实了完整蛋白表达的缺失，检测到了少量的截断肽片段。（来源：J:158427）
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
