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PRND
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1LG4
Identifiers
Aliases	PRND, DOPPEL, DPL, PrPLP, dJ1068H6.4, prion protein 2 (dublet), prion like protein doppel
External IDs	OMIM: 604263; MGI: 1346999; HomoloGene: 8236; GeneCards: PRND; OMA:PRND - orthologs
Gene location (Human) Chr. Chromosome 20 (human) Band 20p13 Start 4,721,909 bp End 4,728,460 bp
Gene location (Mouse) Chr. Chromosome 2 (mouse) Band 2 F2|2 64.07 cM Start 131,792,781 bp End 131,798,050 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right testis left testis Epithelium of choroid plexus visceral pleura testicle skin of hip parietal pleura body of uterus gallbladder myometrium Top expressed in testicle spermatocyte stomach ventricle of the heart neural tube genital tubercle midgut spermatid Hindgut embryo More reference expression data BioGPS More reference expression data
Gene ontology Molecular function copper ion binding metal ion binding Cellular component anchored component of membrane membrane extracellular region plasma membrane anchored component of external side of plasma membrane Biological process protein homooligomerization cellular copper ion homeostasis acrosome reaction single fertilization Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 23627 26434 Ensembl ENSG00000171864 ENSMUSG00000027338 UniProt Q9UKY0 Q9QUG3 RefSeq (mRNA) NM_012409 NM_001126338 NM_001278257 NM_001278520 NM_023043 RefSeq (protein) NP_036541 NP_001119810 NP_001265186 NP_001265449 NP_075530 Location (UCSC) Chr 20: 4.72 – 4.73 Mb Chr 2: 131.79 – 131.8 Mb PubMed search
Wikidata
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Prion protein 2 (dublet), also known as PRND, or Doppel protein, is a protein which in humans is encoded by the PRND gene.

Function

This gene is found on chromosome 20, approximately 20 kbp downstream of the gene encoding cellular prion protein, to which it is biochemically and structurally similar. The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that is found predominantly in testis. Mutations in this gene may lead to neurological disorders.

References

1. ^ GRCh38: Ensembl release 89: ENSG00000171864 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000027338 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. ^ "Entrez Gene: PRND prion protein 2 (dublet)".

Further reading

• Moore RC, Lee IY, Silverman GL, et al. (1999). "Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel". J. Mol. Biol. 292 (4): 797–817. doi:10.1006/jmbi.1999.3108. PMID 10525406.
• Weissmann C, Aguzzi A (1999). "Perspectives: neurobiology. PrP's double causes trouble". Science. 286 (5441): 914–5. doi:10.1126/science.286.5441.914. PMID 10577243. S2CID 82058626.
• Peoc'h K, Guérin C, Brandel JP, et al. (2000). "First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases". Neurosci. Lett. 286 (2): 144–8. doi:10.1016/S0304-3940(00)01100-9. PMID 10825657. S2CID 34958840.
• Lu K, Wang W, Xie Z, et al. (2000). "Expression and structural characterization of the recombinant human doppel protein". Biochemistry. 39 (44): 13575–83. doi:10.1021/bi001523m. PMID 11063595.
• Schröder B, Franz B, Hempfling P, et al. (2001). "Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders". Hum. Genet. 109 (3): 319–25. doi:10.1007/s004390100591. PMID 11702213. S2CID 12262729.
• Moore RC, Mastrangelo P, Bouzamondo E, et al. (2002). "Doppel-induced cerebellar degeneration in transgenic mice". Proc. Natl. Acad. Sci. U.S.A. 98 (26): 15288–93. doi:10.1073/pnas.251550798. PMC 65022. PMID 11734625.
• Deloukas P, Matthews LH, Ashurst J, et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865–71. Bibcode:2001Natur.414..865D. doi:10.1038/414865a. PMID 11780052.
• Peoc'h K, Serres C, Frobert Y, et al. (2003). "The human "prion-like" protein Doppel is expressed in both Sertoli cells and spermatozoa". J. Biol. Chem. 277 (45): 43071–8. doi:10.1074/jbc.M206357200. PMID 12200435.
• Infante J, Llorca J, Rodero L, et al. (2003). "Polymorphism at codon 174 of the prion-like protein gene is not associated with sporadic Alzheimer's disease". Neurosci. Lett. 332 (3): 213–5. doi:10.1016/S0304-3940(02)00941-2. PMID 12399017. S2CID 20222941.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Makrinou E, Collinge J, Antoniou M (2003). "Genomic characterization of the human prion protein (PrP) gene locus". Mamm. Genome. 13 (12): 696–703. doi:10.1007/s00335-002-3043-0. PMID 12514748. S2CID 7755848.
• Peoc'h K, Volland H, De Gassart A, et al. (2003). "Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt–Jakob disease". FEBS Lett. 536 (1–3): 61–5. doi:10.1016/S0014-5793(03)00012-7. PMID 12586339. S2CID 40318359.
• Lührs T, Riek R, Güntert P, Wüthrich K (2003). "NMR structure of the human doppel protein". J. Mol. Biol. 326 (5): 1549–57. CiteSeerX 10.1.1.324.7443. doi:10.1016/S0022-2836(02)01471-7. PMID 12595265.
• Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
• Hundt C, Weiss S (2004). "The prion-like protein Doppel fails to interact with itself, the prion protein and the 37 kDa/67 kDa laminin receptor in the yeast two-hybrid system". Biochim. Biophys. Acta. 1689 (1): 1–5. doi:10.1016/j.bbadis.2004.02.003. PMID 15158907.
• Massimino ML, Ballarin C, Bertoli A, et al. (2005). "Human Doppel and prion protein share common membrane microdomains and internalization pathways". Int. J. Biochem. Cell Biol. 36 (10): 2016–31. doi:10.1016/j.biocel.2004.03.002. PMID 15203115.
• Yin SM, Sy MS, Yang HY, Tien P (2004). "Interaction of Doppel with the full-length laminin receptor precursor protein". Arch. Biochem. Biophys. 428 (2): 165–9. doi:10.1016/j.abb.2004.06.003. PMID 15246873.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Serres C, Peoc'h K, Courtot AM, et al. (2006). "Spatio-developmental distribution of the prion-like protein doppel in Mammalian testis: a comparative analysis focusing on its presence in the acrosome of spermatids". Biol. Reprod. 74 (5): 816–23. doi:10.1095/biolreprod.105.047829. PMID 16421231. S2CID 40554096.
• Azzalin A, Del Vecchio I, Ferretti L, Comincini S (2007). "The prion-like protein Doppel (Dpl) interacts with the human receptor for activated C-kinase 1 (RACK1) protein". Anticancer Res. 26 (6B): 4539–47. PMID 17201176.

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