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中文
CRISPR/Cas9技术通过sgRNA5'-GAGGATGGGCAGGGTCCCGC-3设计，产生了一个17个碱基对的缺失（两处上划线表示删除，下划线部分为野生型序列，即AGGGTCCCGCtggccTGGTGGT）。这个变异发生在exon 1，来源是文献J:344269。
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
