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中文
2-4号外显子被通过同源重组替换为了betageo载体。目标突变导致exon1被连接到betageo载体，产生了所有阅读框的终止密码子。在E18.5时，通过western blot分析检测到纯合突变胚胎，它们不表达Nup50蛋白。(来源：J:63241)
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
