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中文
Exon 3被替换为一个修改过的exon，包含AC替换为CT的核苷酸变异，导致第368位氨基酸由Alanine变为Aspartic Acid（D368A）。通过Flp介导的重组，去除了含FRT标记的诺卡因抗性基因元件。（来源：J:259583）
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
