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中文
这个来自TCPR1577项目的等位基因是在表观基因组学中心通过电穿孔，将Cas9核糖核酸蛋白复合物与单链向导RNA配对，其中5'端的引导序列是ATTATCTCACGTTAGCCGCA，3'端的则是CTCTCCTGTGTGCGTACAGA。这些设计针对的是chr11染色体87729778-87730370的某个关键区域，产生了长度为593bp的缺失（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
