Log In|Sign Up
中文
这种突变是一个从基因组第1888位开始的连续4个鸟嘌呤(G)的缺失，缺失了1个G。预测这会导致一个移位的密码子，使得在删除位置下游10个密码子的位置出现终止密码子。这种突变会导致预测蛋白质缺少参与生物活动的必需氨基酸。(来源：J:2964)
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
