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中文
这个等位基因是一个LINE 1部分重复元素的插入，插入到了基因的一个内含子中。这个插入仅包含元素的最末端1097bp，导致了框架移位变异，预测会生成一个缺失最后1442个氨基酸的截短蛋白质。(来源：J:33734, J:41243)
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
