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中文
通过Cre介导的Nintm1c(EUCOMM)Hmgu等位基因的去除，导致了exon 2的缺失。免疫印迹和免疫染色的检测确认了胚胎纤维细胞和皮肤切片中均无蛋白表达。欲了解针对此类IKMC等位基因的其他靶向策略，请访问http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml(来源：J:277726)。
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
