Log In|Sign Up
中文
在编码蛋白的第22外显子被替换为一个修改过的版本，其中的核苷酸替换导致第892位的氨基酸由asp转换为asn(替换为p.D892N)。这个突变预测会产生无活性激酶。插入在第21内含子的loxP序列引导的诺卡因抗性基因座，随后通过Cre介导的重组被去除了。(来源：J:195237)
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
