Log In|Sign Up
中文
这个等位基因是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列（GATAAATAACCGAAGCACTG, GCAAAACCTGGACCAGTAGA）产生的，导致了10号染色体（Chr10）5,841,189-5,841,728区段的540bp缺失，具体位置是GRCm38/mm10系统。这个缺失事件去除了基因ENSMUSE00000097978的全部外显子（J:188991）。
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
