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中文
CRISPR/Cas9基因编辑技术用于在NC_000069.6的第16外显子154939648-651位插入一个4个碱基的缺失，导致丝氨酸532后产生移码，并在29个异常域下游位置产生终止。(来源：J:280429)
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
