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中文
一段跨越exon 1，包含可能的转录起始点和翻译起始位点的片段被替换为PGK-HPRT。突变的MEFs的Northern和Western印迹实验确认了mRNA和蛋白质表达的缺失(来源：J:97640)。
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
