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中文
在exon 6的arginine第355位（CGA）被替换成了终止密码子（TGA），通过sgRNA和ssODN模板，使用了CRISP/Cas9技术。这个突变等同于人类的p.R359*变异，与血小板减少症5型（T5）相关（参考文献：J:342774）。
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
