The transgenic construct contains an untagged human profilin 1 (PFN1) cDNA sequence (420 bp) encoding the G118V mutant protein under the direction of mouse prion protein promoter. The G118V mutation is associated familial amyotrophic lateral sclerosis (fALS). Expression is detected in brain, spinal cord, and to a lesser extent in skeletal muscle. The transgene is not expressed in the liver. Founder line 838 was identified with total PFN1 protein levels in spinal cord at ~5-fold greater levels compared to endogenous mouse PFN1 protein levels in non-transgenic mice. The transgene inserted on chromosome 12 causing a 151 kb deletion in the Mdga2 (exons 2-3) gene, it is not known if insertion generated a null allele in Mdga2. (J:101977, J:241428)
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基础信息

模型ID
品系来源
等位基因类型
突变
遗传方式
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参考文献
C57BL/6N
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Insertion, Intragenic deletion
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1
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3

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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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N: 正常表型
(#): 上标括号内为相关疾病数量
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