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中文
CRISPR/Cas基因编辑技术用于在基因组序列的exon 1中产生166个核苷酸的缺失，导致在exon 2处提前终止。通过OTOP1抗体的免疫染色，确认了纯合突变体中OTOP1蛋白的缺失（来源：J:293042）。
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
