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通过Cre介导的父本1700010I14Riktm2a(KOMP)Wtsi等位基因的去除，去除了由启动子驱动的诺卡因选择标记片段，以及关键的内含子，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靶向策略的更多信息，可访问http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml(来源：J:204739)。
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
