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中文
CRISPR/cas9基因编辑通过一个信号导向RNA，设计用于在exon 10插入一个115个核苷酸的缺失突变。这个缺失是(CTGCTCCTGCTCTAGaaaagctacgtgcc/del115/acgctcatgtttggacagcgGTCAGTATCAGA;下划线部分是exon 10序列，上方为内含子DNA的上界)。来源：(J:101977)
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
