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中文
CRISPR/Cas9技术通过sgRNA(靶向ACTTCTTCCGGAATGCACTG)和ssODN模板，产生了一个116bp的缺失，这个缺失包含了W323编码区域以及前一个内含子的部分，导致了完全的表达丢失，经 Western blot 分析确认。(来源：J:332442)
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
