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中文
部分exon4和exons5-7被替换了抗氨苄青霉素抗性基因，通过同源重组，导致最后一个锌指域及整个TRAF域的缺失。通过E12.5胚胎来源的鼠胚胎成纤维细胞（MEFs）的 Western blot分析，证实了纯合突变体中基因表达缺失。（来源：J:76067）
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
