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中文
CRISPR/cas9技术引发了基因编辑，导致1个位于exon 1的2个碱基GG缺失(48837539-48837540)，1个位置48837541的G-C替换，以及exon 7中3个碱基CAC的删除(48849905-48849907)。这个等位基因产生了截短的蛋白质。(来源：J:296988)
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
