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中文
这个等位基因缺失了2号和3号外显子，它们编码DNA结合的高移动性组域和全部转录激活域。它可以通过Cre重组酶剔除Sox9tm1Gsr中包含2号和3号外显子的loxP标记区域，或者通过同时去除2号和3号外显子以及Sox9tm2Gsr中含loxP标记的neo cassette（Sox9tm1Gsr中已删除）来产生（来源：J:75124）。
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
