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中文
Exon 1和下游部分内含子被替换成lacZ-neo载体，通过同源重组实现。北半球杂交分析，使用针对15-620核苷酸的cDNA探针，证实了E9.5纯合突变胚胎中基因表达的缺失。（来源：J:75477）
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
