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中文
这个来自TCPR1002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GTACCAGTCATGCTCCGCCA(5'端)和CTGTATATTCTGACGGACAA(3'端)特定引物的Cas9核糖核酸同质体，目标是chr17:63981519至63981658的位置，导致了140bp的染色体片段缺失。(GRCm38参考序列，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
