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中文
这种C到A的无义突变将密码子27从丝氨酸(TCG)变为终止密码子(TAG)，导致SW:Q6R3M4基因的p.S27*变异。由此产生的蛋白质会缺失催化功能，是一个截短的产物。这个突变在分析的129个纯系中普遍存在，包括129P3/J、129X1/SvJ、129P1/ReJ和129P2/Ola。C57BL/6J和BALB/c小鼠不含有这个突变。(引用文献：J:85061, J:228234, J:273998)
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
