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中文
CRISPR/Cas9技术针对c.379G至c.396C区域进行了编辑，产生了缺失等位基因。这项记录汇总了两条线的数据，一条线在这个区域有2个碱基的缺失，导致移位和早停密码子，另一条线有8个碱基的缺失。这模拟了人类中常见的c.391dup（p.Met131Asnfs*3）变异。来源：J:326462
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
