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中文
4-6号外显子被替换成一个含loxP标记的诺卡因选择座。这个缺失预计会导致在第195位氨基酸后发生阅读框跳跃，并产生一个终止密码子，如果3号外显子连接到7号外显子。表达的突变蛋白将只有一个锌指结构，但不包含螺旋环域。(来源：J:260445)
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
