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中文
开放阅读框被替换为一个带有核定位信号的无启动子lacZ基因，以及一个由Cre介导的Cre重组后去除的floxed PGK-hprt元件。转录缺失通过在胎盘和皮肤组织的Northern blot分析中得到确认。(来源：J:128922)
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
