Log In|Sign Up
中文
大约80%的编码区域被同源重组插入的诺卡因选择座替换。删除区域包含推测的膜穿孔区域。通过北向 blot 对大脑组织的分析，该转录本在纯合突变小鼠中未检测到。基于胆红素生成的检测方法显示，纯合突变小鼠功能完全丧失。(来源：J:29523)
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
