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中文
在橡树岭国家实验室创造的一种诱导突变，发生在 intron 14 的 +1 位点的一个 G 变为 A，导致从这个等位基因表达的转录本中删除了 exon 14。缺失的序列编码潜在的第五个跨膜域。（来源：J:38977）
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
