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中文
使用包含Sox10调控区的BAC，将人类雌激素受体(ERT2)的突变配体结合域与Cre重组酶编码序列连接，并直接插入转录起始点下游。在BAC两侧的LoxP位点在微注射前被去除。Sox10调控区驱动CreERT2重组酶在神经管特异性表达。(来源：J:299312)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
