PRND

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
Gene location (Human)
Chr.	Chromosome 20 (human)
End	4,728,460 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	131,798,050 bp
RNA expression pattern
	Top expressed in
	visceral pleura; ; parietal pleura; ; gallbladder; ; myometrium; ; smooth muscle tissue; ; ganglionic eminence; ; endometrium; ; thymus; ; stromal cell of endometrium; ; renal cortex;
	Top expressed in
	testicle; ; spermatocyte; ; stomach; ; ventricle; ; neural tube; ; midgut; ; spermatid; ; Hindgut; ; quadriceps femoris muscle; ; white adipose tissue;
	More reference expression data
	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
	23627
	26434
	ENSG00000171864
	ENSMUSG00000027338
	Q9UKY0
	Q9QUG3
	NM_012409
	NM_001126338 ; NM_001278257 ; NM_001278520 ; NM_023043
	NP_036541
	NP_001119810 ; NP_001265186 ; NP_001265449 ; NP_075530
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated December 28, 2023

Prion protein 2 (dublet), also known as PRND, or Doppel protein, is a protein which in humans is encoded by the PRND gene.^[5]

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.^[5]

Related Research Articles

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References

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

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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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000171864 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 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.

[entrez-5] 1 2 "Entrez Gene: PRND prion protein 2 (dublet)".

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[5]

PRND

Contents

Function

Related Research Articles

References

Further reading