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中文
Exon 7被Cre介导的重组移除，导致了框移翻译。通过使用位于exon 6和9的RT-PCR引物，我们确认了小鼠胚胎成纤维细胞中野生型等位基因的缺失。然而，产生了更多不包含exons 7和8的替代剪接形式，这个版本缺失了TRAF2和NEMO的结合位点。(来源：J:126113)
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
