Log In|Sign Up
中文
使用CRISPR/Cas9技术，针对exons 1和2设计了gRNAs。这个等位基因代表了线号14，它在exon 2存在一个8个碱基的缺失。通过胸腺、脾脏和MEFs的蛋白质提取物进行 Western blotting 实验后，观察到了这个等位基因的表达缺失。（来源：J:274050）
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
