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中文
这个基因通过同源重组在第181位密码子插入了耐药性质粒，导致其功能受损。在纯合突变动物的肝脏、脾脏、乳腺、胸腺、肾脏和骨骼肌中，通过Northern和Western印迹分析证实了基因表达的缺失(来源：J:41784)。
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
