Log In|Sign Up
中文
CRISPR/Cas9介导的重组在exon 1产生了一个8个碱基的缺失(GGCCTGAG)。 Western blot分析证实了纯合小鼠中蛋白质表达的缺失(来源：J:265543, J:326577)。
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
