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中文
大多数exon 2被删除，并通过同源重组替换为诺卡因抗性基因座。exon 2编码开放阅读框的除71个核苷酸之外的所有序列。通过在15日龄同源突变动物脑组织的原位杂交分析，确认了基因表达的缺失。(来源：J:71116)
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
