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中文
删除了编码27-301个氨基酸的3.4千碱基基因，并通过同源重组替换为PGK-neo载体。通过电泳迁移率测定(EMSA)和野生型小鼠胚胎成纤维细胞(nuclear extracts)的 Western blot分析，证实了纯合突变体中基因表达的缺失。(来源：J:46788)
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
