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中文
CRISPR/cas9通过gRNAs（GGCTCTCCACTTCTAGCTAC和CAACGGATCTTATGAGTTC）引起的一种编辑，产生了一个13,432bp的缺失和一个单个碱基的插入（T），这个区域与人类acheiropodia患者中一个12kb的缺失区域有同源性。（来源：J:306058）
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
