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中文
这个基因通过同源重组的方式，用一个诺卡因抗性质粒替换了编码494-619氨基酸（包括C1区域）的4个外显子，从而被打乱。通过 Western blot 用针对蛋白质极端N端和C端的抗体进行了缺失等位基因的验证。（来源：J:56513）
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
