Log In|Sign Up
中文
Mybtm1Cgn与小鼠在由人CMV驱动的Cre载体控制下交叉，该载体剪除了exon 2，留下一个LoxP位点。Southern blot确认了重组，而胎肝的Western blot结果显示突变体中缺乏蛋白。(来源：J:91122)
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
