Log In|Sign Up
中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和指导序列TGGATACCCCCATATCCGCA和CGGAGGCTCCTAGTCCCACG产生的，导致了从染色体2的30,471,400bp开始，到30,474,456bp之后的3057bp区域的缺失。这个变异删除了ENSMUSE00000462138（第1个外显子）以及374bp的内含子序列，包括转录起始点，预测会成为一个无功能的等位基因。（来源：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
