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中文
内源性等位基因在插入包含9到13号外显子、选择基因以及11号内含子11处300bp缺失的载体后被干扰。通过载体的同源重组，产生了双链断裂修复的等位基因，特征是13号外显子后面跟着选择基因，9到13号外显子有重复。通过睾丸和脾脏组织的RT-PCR分析，杂合突变小鼠中未检测到转录本。邻近基因Vrk2的表达未受影响。（来源：J:80424）
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：
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| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
