Log In|Sign Up
中文
内源性等位基因的Exon 3通过同源重组被neo抗性基因座的插入所打断。这个缺失区域编码G1和G2的GTP酶域序列。插入在Exon 3的5'端引入了一个终止密码子，导致在同源突变胚胎的 Western blot 分析中未检测到蛋白质。(来源：J:81438)
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
