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中文
通过Cre介导的父本Ubxn7tm1a(EUCOMM)Wtsi基因座的去除，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，保留了插入的lacZ报告序列。欲了解针对此类IKMC基因座以及其他类似基因的靶向策略详情，请访问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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
