Log In|Sign Up
中文
一个包含整个编码区域的4.5kb片段通过同源重组被一个诺卡因选择标记的载体替换。通过来自纯合突变小鼠来源的星形胶质细胞的Northern blot分析未检测到转录本。蛋白质缺失通过2D-PAGE得到了验证。(来源：J:77283)
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
