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中文
在Exon 1，编码起始翻译位点的部分，通过同源重组被诺美西林筛选 cassette 替换。对纯合突变小鼠大脑总RNA的RT-PCR结果显示，目标位点处无转录本产生。编码蛋白的缺失通过脑匀浆的Western blot分析和冠状切片的免疫细胞化学检测得到了确认。(来源：J:78649)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
