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中文
在Furin上游，针对NKX2-5结合增强子M10设计了两个sgRNAs，目标序列分别为ATGCGGTTGTGATCTCTCGG和GCCACCGGCAAAGGCGTGGT，使用CRISPR/Cas9技术后，成功实现了676行的896bp缺失(来源：J:273415)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
