Log In|Sign Up
中文
Atoh1增强子Eh2或E3通过CRISPR/Cas9技术，用sgRNAs针对TATGAACTAGAATATTGTATTGG和AACGTATTCAAAGTCAAAGCGGG位点进行了编辑，产生了包含增强子的2519bp缺失，位置在chr6:64774536-64777054（GRCm39）。(引用信息：J:332270, J:333396)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
