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中文
构建了一个靶向载体，通过同源重组在ES细胞中将Cre/ERT2编码序列、poly(A)信号和Frt标记的neo选择座插入Notch 4的起始密码子附近。这导致了exon 1的大部分被删除。随后，杂合雄性与Flpe表达的雌性杂交，以去除选择座。(来源：J:179632)
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
