人 PRNP (NM_183079) cDNA克隆

Accession: NM_183079
基因名称: PRNP
基因别名: CJD; GSS; PrP; ASCR; KURU; PRIP; PrPc; CD230; AltPrP; p27-30; PrP27-30; PrP33-35C
基因描述: Homo sapiens prion protein (PRNP), transcript variant 2, mRNA.
种属: Human
CDS区长度: 762 (查看编码区序列)
翻译后氨基酸长度: 253 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an alternate splice site in the 5' UTR compared to variant 1. Variants 1-5 encode the same protein.
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G100835 人 PRNP (NM_183079) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]