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中文
分子分析显示，Exon 3存在一个7个碱基的缺失，导致一个43个氨基酸的移位，并在第308位产生一个过早终止。由此产生的蛋白质缺失了C端的6个跨膜域。(来源：J:73642)
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
