The insertion of sequence encoding GFP into exon 3 resulted in the generation of a hypomorphic allele lacking exon 3. Though the floxed neo cassette used for selection was excised, inverted repeats at the insertion site of the remaining loxP site may be the reason for the aberrant splicing. Mutant transcript was detected by Northern blot, RT-PCR, and RNase protection. Sequence analysis of the RT-PCR products showed that exon 2 spliced directly to exon 4, producing a transcript lacking exon 3 similar to a splice variant found at low levels in wild-type mice. The transcript putatively encodes protein lacking 154 residues from the N-terminal domain, but containing the nuclear localization signal and DNA-binding and C-terminal acidic activation domains. (J:86255)
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基础信息

模型ID
品系来源
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突变
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Insertion
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1
4
5

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标签摘要:
hm: 纯合子
ht: 杂合子
cn: 条件基因型
cx: 复合型:涉及多基因组
tg: 转基因
ot: 其他:半合子、不确定...
(F): 雌性
(M): 雄性
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(#): 上标括号内为相关疾病数量
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