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插入的PGK_EM7_PuDtk_bGHpA片段导致了182个碱基的缺失，起始于11号染色体(Genome Build 37)的96,126,438位置，终止于96,126,620。这个缺失消除了对应的小miRNA的DNA序列。该片段由一个loxP位点、一个F3位点、一个PGK-puromycin-delta-tk cassette、另一个loxP位点以及最终的FRT位点组成。通过Cre介导的重组，选择性片段被移除了。(来源：J:226712)
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
