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中文
通过同位素标记的定点突变技术，将536位的谷氨酸（Glu）替换为异亮氨酸（Ala），产生了等同于人类GUS缺陷中活性位点的氮原子替换突变（E540A，E536A）。这位于第十号外显子。来源：(J:81792)
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
