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中文
这个基因通过同源重组，用诺卡因抗性载体替换了1号和2号外显子，以及1.6千碱基的5'上游序列。基因表达缺失通过来自纯合突变胚胎胚胎成纤维细胞的 Western blot 分析得到了确认(来源：J:47300)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
