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中文
Exon 2被替换为一个带有frt标记的neo cassette，该元件在转录时会被阅读。这导致exon3产生一个终止密码子。蛋白质产物的缺失通过免疫组化在脑组织切片中得到了确认(来源：J:135586, J:139493)
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
