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中文
北卡罗来纳州立大学等位基因的序列分析显示，第12外显子存在一个单核苷酸缺失。这一缺失导致阅读框的移位，随后产生11个氨基酸的替换，并在跨膜域之前提前终止了蛋白质。(来源：J:60363)
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
