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中文
这个基因通过同源重组的方式，用PGK-neo cassette替换了exon 2，导致其功能受损。通过在来自纯合突变体的胚胎成纤维细胞中进行 Western blot 分析，确实证实了基因表达的缺失。（来源：J:83559）
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
