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中文
Tc-3H这一等位基因是由7号外显子末尾的一个splice donor突变引起的。预测会导致蛋白质部分缺失，或者由于捐赠位点的read-through导致344氨基酸之后的开放阅读框发生改变（来源：J:93195）。
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
