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中文
通过同源重组，422bp的5'非编码区和144bp的基因编码区被PGK-neo cassette替换。这种基因靶向事件导致基本 helix-loop-helix 区域的前48个氨基酸缺失。在同位素标记的实验中，同源突变动物肾脏内的基因表达缺失。(来源：J:76787)
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
