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中文
该位置的第二个锌指，由第3号外显子编码，被核受体亚家族3，组C，成员1的第4号外显子替换，形成一个嵌合蛋白。载体下游包含了条件性Cre介导的删除的floxed neo序列。（来源：J:120102）
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
