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中文
通过同源重组，将人类cDNA编码EGFR插入了内源性位置。下游插入了一个RSV-neo载体。在脑组织的RNA酶保护实验中检测到了人类转录本的内源性水平，但在骨和上皮组织中观察到了部分失活表达，可能与下游的neo载体有关。（来源：J:84870）
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
