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中文
在exon 1前方3.7千碱基的位置插入了一个loxP位点。随后，一个带有floxed neo cassette的片段被插入在exon 1之后。通过Cre介导的重组，neo cassette被剔除了，留下包含Prader-Willi综合症印记中心（PWS-IC）的6千碱基区域，这个区域现在是floxed的。（来源：J:174457）
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 |
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References Literature
Title
PMID
Journal
Year
IF
