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中文
这个基因陷阱载体插入到了贡献相等于完整SH2域的两个外显子之间。预测显示SH2域在第74位氨基酸位置会被截断，导致SH2功能丧失。Northern blot和RT-PCR确认了突变体中野生型转录本的缺失。（来源：J:110009）
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
