Log In|Sign Up
中文
通过Cre介导的父本Rsf1tm1a(EUCOMM)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。欲了解针对此类IKMC等位基因以及其他类似策略的更多信息，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
