这个敲除报告基因是由Cre重组酶从Bsph1tm1Osb衍生出来的,它缺失了内源基因的第4和部分第5外显子,保留了靶向构建(KOMP向量HTGRS6004_A_H09)中的lacZ报告基因(由内源性启动子驱动),周围带有1个FRT和1个loxP位点。(来源:J:94077)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6NSlc-Tg(CAG-EGFP,Acr-EGFP)2Osb
Targeted
插入,基因内删除
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1
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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
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