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中文
在18号染色体的37,896,093位碱基(位置v38)或NC_000084基因组区域的39,542位，由于ENU诱导的T到A替换。这个变异在cDNA和蛋白质水平的影响尚未研究，但预测会导致exon 11的缺失，exon 11总共有28个。exon 11的跳过会导致第348位之后的框架移位蛋白质产物，并在第348位后提前终止。信息来源：J:254819
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
