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中文
这个等位基因是在表型基因组学中心通过电穿孔方式，用含有CTAATATTACGCTTGAAAGT和GTGCCTGACTGTAGATGAGA这些 Spacer序列的Cas9 RNA和引导RNA构建的。通过将包含loxP位点、间隔序列和邻近同源臂的单一修复模板，通过胚胎与重组AAV的孵育来递送。这个产生的等位基因在ENSMUSE00000513987（GRCm39）外显子周围有loxP位点。预测使用Cre酶介导的删除会去除这个loxP标记区域，从而产生一个无功能的等位基因。（来源：J:345353）
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 |
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References Literature
Title
PMID
Journal
Year
IF
