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中文
这个来自TCPR1036项目的等位基因是在表型遗传学中心通过电穿孔，使用了带有CATAGGGGTCTGGTGATCTA和GAGGGTTCCCCACTGCCAAT的单导RNA，针对7号染色体5'端以及CGTGTCAGGACATCCACCAC和GCGGAACTTGCTCATGGAAC的3'端，针对一个关键区域进行的。这导致了7号染色体127,608,671到127,612,386位置的3,716bp缺失；(预测的对蛋白p.P84X的影响)(GRCm38参考)(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
