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中文
一种由CRISPR/Cas9技术引入的T>A替换(c.362T>A)，导致第121位的异亮氨酸密码子变为天冬酰胺密码子(p.I121N)，这模拟了Charcot-Marie-Tooth病患者中发现的p.I122N变异。(来源：J:283448)
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
