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中文
在第17外显子的第729位，将丝氨酸替换为阿尔法氨基酸(苏729A)的改变引入，之后在第17外显子下游插入了一个FRT引导的诺卡因选择标记。通过Flp介导的重组移除了这个选择标记。(来源：J:261443)
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 |
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References Literature
Title
PMID
Journal
Year
IF
