^ abcGRCh38: Ensembl release 89: ENSG00000129255 - Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000018761 - 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.
^Ware FE, Lehrman MA (Aug 1996). "Expression cloning of a novel suppressor of the Lec15 and Lec35 glycosylation mutations of Chinese hamster ovary cells". J Biol Chem. 271 (24): 13935–8. doi:10.1074/jbc.271.24.13935. PMID 8663248.
^Mao M, Fu G, Wu JS, Zhang QH, Zhou J, Kan LX, Huang QH, He KL, Gu BW, Han ZG, Shen Y, Gu J, Yu YP, Xu SH, Wang YX, Chen SJ, Chen Z (Aug 1998). "Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning". Proc Natl Acad Sci U S A. 95 (14): 8175–80. Bibcode:1998PNAS...95.8175M. doi:10.1073/pnas.95.14.8175. PMC20949. PMID 9653160.
^Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Korn-Lubetzki I, Revel-Vik S, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M (Dec 2001). "MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If". J Clin Invest. 108 (11): 1687–95. doi:10.1172/JCI13419. PMC200989. PMID 11733564.
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Zhang QH, Ye M, Wu XY, et al. (2001). "Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells". Genome Res. 10 (10): 1546–60. doi:10.1101/gr.140200. PMC310934. PMID 11042152.
Anand M, Rush JS, Ray S, et al. (2001). "Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammals". Mol. Biol. Cell. 12 (2): 487–501. doi:10.1091/mbc.12.2.487. PMC30958. PMID 11179430.
Kranz C, Denecke J, Lehrman MA, et al. (2002). "A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)". J. Clin. Invest. 108 (11): 1613–9. doi:10.1172/JCI13635. PMC200991. PMID 11733556.
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. PMC139241. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Suzuki Y, Yamashita R, Shirota M, et al. (2004). "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions". Genome Res. 14 (9): 1711–8. doi:10.1101/gr.2435604. PMC515316. PMID 15342556.
Pope SN, Lee IR (2005). "Yeast two-hybrid identification of prostatic proteins interacting with human sex hormone-binding globulin". J. Steroid Biochem. Mol. Biol. 94 (1–3): 203–8. doi:10.1016/j.jsbmb.2005.01.007. PMID 15862967. S2CID 9746088.
Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC1847948. PMID 17353931.
External linksedit
GeneReviews/NCBI/NIH/UW entry on Congenital Disorders of Glycosylation Overview
This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it.
mpdu1, mannose, dolichol, utilization, defect, protein, protein, that, humans, encoded, gene, identifiersaliases, cdgif, hbebp2bpa, lec35, my008, pp3958, pqlc5, sl15, mannose, dolichol, utilization, defect, slc66a5external, idsomim, 604041, 1346040, homologene. Mannose P dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene 5 6 7 8 MPDU1IdentifiersAliasesMPDU1 CDGIF HBEBP2BPA Lec35 My008 PP3958 PQLC5 SL15 mannose P dolichol utilization defect 1 SLC66A5External IDsOMIM 604041 MGI 1346040 HomoloGene 3581 GeneCards MPDU1Gene location Human Chr Chromosome 17 human 1 Band17p13 1Start7 583 529 bp 1 End7 592 789 bp 1 Gene location Mouse Chr Chromosome 11 mouse 2 Band11 B3 11 42 86 cMStart69 547 523 bp 2 End69 553 468 bp 2 RNA expression patternBgeeHumanMouse ortholog Top expressed inrectumislet of Langerhansright lobe of liverleft adrenal glandgallbladderbody of stomachganglionic eminencemonocyteright lobe of thyroid glandupper lobe of left lungTop expressed inyolk saclipmorulaankle jointduodenumproximal tubulesuperior frontal gyrusesophagusbrown adipose tissuestomachMore reference expression dataBioGPSMore reference expression dataGene ontologyMolecular functionprotein bindingCellular componentintegral component of membrane extracellular exosome endoplasmic reticulum membrane membrane mitochondrion endoplasmic reticulumBiological processdolichol linked oligosaccharide biosynthetic process oligosaccharide biosynthetic process protein folding transportSources Amigo QuickGOOrthologsSpeciesHumanMouseEntrez952624070EnsemblENSG00000129255ENSMUSG00000018761UniProtO75352Q9R0Q9RefSeq mRNA NM 004870NM 001330073NM 001301710NM 001301711NM 011900RefSeq protein NP 001317002NP 004861n aLocation UCSC Chr 17 7 58 7 59 MbChr 11 69 55 69 55 MbPubMed search 3 4 WikidataView Edit HumanView Edit Mouse Contents 1 See also 2 References 3 Further reading 4 External linksSee also editDolichol monophosphate mannose Congenital disorder of glycosylationReferences edit a b c GRCh38 Ensembl release 89 ENSG00000129255 Ensembl May 2017 a b c GRCm38 Ensembl release 89 ENSMUSG00000018761 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 Ware FE Lehrman MA Aug 1996 Expression cloning of a novel suppressor of the Lec15 and Lec35 glycosylation mutations of Chinese hamster ovary cells J Biol Chem 271 24 13935 8 doi 10 1074 jbc 271 24 13935 PMID 8663248 Mao M Fu G Wu JS Zhang QH Zhou J Kan LX Huang QH He KL Gu BW Han ZG Shen Y Gu J Yu YP Xu SH Wang YX Chen SJ Chen Z Aug 1998 Identification of genes expressed in human CD34 hematopoietic stem progenitor cells by expressed sequence tags and efficient full length cDNA cloning Proc Natl Acad Sci U S A 95 14 8175 80 Bibcode 1998PNAS 95 8175M doi 10 1073 pnas 95 14 8175 PMC 20949 PMID 9653160 Schenk B Imbach T Frank CG Grubenmann CE Raymond GV Hurvitz H Korn Lubetzki I Revel Vik S Raas Rotschild A Luder AS Jaeken J Berger EG Matthijs G Hennet T Aebi M Dec 2001 MPDU1 mutations underlie a novel human congenital disorder of glycosylation designated type If J Clin Invest 108 11 1687 95 doi 10 1172 JCI13419 PMC 200989 PMID 11733564 Entrez Gene MPDU1 mannose P dolichol utilization defect 1 Further reading editMaruyama K Sugano S 1994 Oligo capping a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides Gene 138 1 2 171 4 doi 10 1016 0378 1119 94 90802 8 PMID 8125298 Suzuki Y Yoshitomo Nakagawa K Maruyama K et al 1997 Construction and characterization of a full length enriched and a 5 end enriched cDNA library Gene 200 1 2 149 56 doi 10 1016 S0378 1119 97 00411 3 PMID 9373149 Zhang QH Ye M Wu XY et al 2001 Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34 hematopoietic stem progenitor cells Genome Res 10 10 1546 60 doi 10 1101 gr 140200 PMC 310934 PMID 11042152 Anand M Rush JS Ray S et al 2001 Requirement of the Lec35 gene for all known classes of monosaccharide P dolichol dependent glycosyltransferase reactions in mammals Mol Biol Cell 12 2 487 501 doi 10 1091 mbc 12 2 487 PMC 30958 PMID 11179430 Kranz C Denecke J Lehrman MA et al 2002 A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If CDG If J Clin Invest 108 11 1613 9 doi 10 1172 JCI13635 PMC 200991 PMID 11733556 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 Ota T Suzuki Y Nishikawa T et al 2004 Complete sequencing and characterization of 21 243 full length human cDNAs Nat Genet 36 1 40 5 doi 10 1038 ng1285 PMID 14702039 Suzuki Y Yamashita R Shirota M et al 2004 Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions Genome Res 14 9 1711 8 doi 10 1101 gr 2435604 PMC 515316 PMID 15342556 Pope SN Lee IR 2005 Yeast two hybrid identification of prostatic proteins interacting with human sex hormone binding globulin J Steroid Biochem Mol Biol 94 1 3 203 8 doi 10 1016 j jsbmb 2005 01 007 PMID 15862967 S2CID 9746088 Ewing RM Chu P Elisma F et al 2007 Large scale mapping of human protein protein interactions by mass spectrometry Mol Syst Biol 3 1 89 doi 10 1038 msb4100134 PMC 1847948 PMID 17353931 External links editGeneReviews NCBI NIH UW entry on Congenital Disorders of Glycosylation Overview nbsp This article on a gene on human chromosome 17 is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title MPDU1 amp oldid 1115909736, wikipedia, wiki, book, books, library,
