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中文
CRISPR/Cas9导向的基因组编辑技术用于在Gm16286(UniProt Q9CQX6)基因的131-225位点创建一个95bp的缺失，这导致了密码子框架的移位，并在第67位产生了一个终止密码子(来源：J:308825)。
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
