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中文
这种突变是在对不育小鼠进行EMS诱变筛选时发现的。分子缺陷在于11号内含子的AG剪接接受序列上的一个A到T的转换。这个等位基因产生了两种异常剪接的转录本，两者都导致了野生型序列的框架移位和早停密码子。 (Source: EMS mutagenesis screen for infertile mice)
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
