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中文
在Sox9结合位点对应的启动子区域引入了点突变。研究表明，这种位点的突变会消除Sox9的结合。在凝胶电泳实验中证实了这一点。随后，一个含loxP标记的诺卡因选择座被放置在内含子1内。(来源：J:58474)
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
