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中文
CRISPR/cas9基因编辑技术用于在第一个编码外显子(Exon 2)插入一个16bp的缺失(指导RNAc.403-422;NM_133840.2;缺失为c.414-429)，产生一个在第139位密码子(425个密码子后)后的框架移位，随后跟着一个终止密码子。(来源：J:311491)
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
