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中文
这种表型突变是在对神经表型进行乙醚甲基磺酸盐(EMS)诱变筛选中发现的。分子缺陷是位于U2一致分支序列(BSRS)的高保守区域，以及BSRS和U2/U6螺旋间5个碱基对的缺失。(来源：J:179357)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
