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中文
这个来自TCPR1017项目的等位基因是在表观基因组学中心通过电穿孔，用带有GTATAACTAGCTGAGCTGAT和TCATAAGTTCCGATCTTGGC这两条单引物RNA，针对16号染色体19701123位点的5'和3'端，用Cas9核酶复合物生成的。这导致了chr16:19701123一个插入型变异，即insT（预测对蛋白p.S104Kfs*4的影响）（GRCm38参考）。信息来源为J:237616。
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
