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中文
这个突变是由TCPR0331项目在TCP通过注入Cas9 mRNA和一个指导RNA带有spacer序列GGGAAGGCAACGGATCGCTG产生的。它导致了chr8:90270347到90270350位置的4个碱基删除，影响了ENSMUSE00000331868基因。这个变异预测会导致从第96位氨基酸开始的框架移位，随后是53个氨基酸的早期截断（p.S96Rfs*55，GRCm38参考）。(来源：J:165963)
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
