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中文
在432位点引入了点突变，由编码亮氨酸的密码子变为脯氨酸，同时在430位点有一个中性突变，产生了一个PvuII酶切位点。此外，还插入了一个位于邻近内含子的loxP引导的诺卡因选择性载体。(来源：J:67930)
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
