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中文
这个转基因包含了人类泛素C启动子驱动的增强型绿色荧光蛋白开放阅读框。转基因插入了17号染色体的29,435,589位点（参考序列NC_000083.6；GRCm38.p6），这是一个靠近H-2染色体着丝粒的非编码区域，距离H-2 K1基因大约4600千碱基对。（来源：J:93490, J:242067, J:287278）
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
