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中文
CRISPR/Cas9基因编辑技术被用来产生一个1306+2bp的缺失，涉及编码区域，包括起始密码子上游23bp，一直到终止密码子上游49bp的位置。(来源：J:337424)
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：
Show/Hide columns
| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
