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中文
CRISPR技术产生的点突变是在第14位由丝氨酸替换为精氨酸(由C变G)，这被称为S14R的氨基酸替换。一个无义突变(由C变T)产生了一个Aat I的限制性酶切位点，以方便遗传型鉴定。(来源：J:291454)
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
