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中文
通过Cre介导的亲本等位基因去除导致了由启动子驱动的诺卡因选择座的消除，留下插入的lacZ报告序列。有关这种IKMC等位基因以及其他类似目标策略的更多信息，请参阅http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml(来源：J:94077)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
