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中文
一段包含exon 3的5kb基因区域通过同源重组被PGK-neo cassette替换，导致DNA结合域的第二个锌指缺失。对纯合突变动物的肠和肾进行RT-PCR分析后，检测到了突变转录本。序列分析显示有一个131bp的缺失，对应于第二个锌指，造成一个移位和下游12bp的无义密码子。(来源：J:42815)
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 |
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References Literature
Title
PMID
Journal
Year
IF
