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中文
CRISPR/Cas9通过设计的sgRNAs靶向exons 2和3，产生了5个碱基的缺失突变(CTTGA)，在exon 3的位置，导致了密码子162的错位突变(从GAC变为)，以及一个在13个密码子后38个核苷酸位置的早停密码子(Asp162Glufs*13)。参考文献：J:322160
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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References Literature
Title
PMID
Journal
Year
IF
