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中文
捐赠者通过体内同源重组技术，在小鼠的3F2.1和3F2.2染色体上构建了含有0.8兆碱基的重复或缺失，这些区域与人类的1q21.1区域具有同源性。简而言之，他们在基因组中插入了loxP位点，以环绕目标的复制/删除区域，随后由Cre酶介导的重组移除了插入序列。（来源：J:94077）
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
