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中文
基因的Exon 2被两个LoxP位点夹持。在成体生殖细胞中，通过Cre介导的重组导致了Exon 2的缺失。 Western blot检测在E11.5同源突变胚胎的心脏中确认了蛋白表达的完全缺失。(来源：J:256653)
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
