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中文
这个来自TCPR1152项目的等位基因是在表观基因组学中心通过电穿孔，使用了针对关键exon5'端CCAGTGGAGTCGGGCGCTCT和3'端ATGGGCGTCTCGACCCGCAC的单引物RNA，伴随Cas9核酸酶复合物生成的，导致一个79bp的缺失，位置在染色体8：95633624到95633702（GRCm38建库）。(J:265051)
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
