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中文
将exons 2和3替换为PGK-neo载体，构建了一个无功能等位基因。通过在大脑、皮肤、肺、心脏和肝脏组织中进行 Western Blot 分析，确认了蛋白产物的缺失。(来源：J:125188)
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
