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中文
一个带有敲除neo cassette的点突变构建产生了1个碱基的缺失，导致了 frameshift和一个在保守的10到15个氨基酸的C端序列下游的早停密码子。 Western blot结果显示，杂合子小鼠中，一个截短蛋白的表达确实减少了。(来源：J:192154)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
