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中文
这个等位基因是通过在重组胚胎干细胞中短暂表达Cre重组酶，从Traf2tm1Rbr中去除3号floxed外显子产生的。去除3号外显子导致了阅读框的移位，并引入了一个早发的终止密码子。(来源：J:93890)
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
