MPDU1

From Wikipedia, the free encyclopedia


Mannose-P-dolichol utilization defect 1
Identifiers
Symbol(s) MPDU1; CDGIF; FLJ14836; HBEBP2BPA; Lec35; PQLC5; SL15
External IDs OMIM: 604041 MGI: 1346040 HomoloGene: 3581
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 9526 24070
Ensembl ENSG00000129255 ENSMUSG00000018761
Uniprot O75352 Q8C9V6
Refseq NM_004870 (mRNA)
NP_004861 (protein)		 XM_991863 (mRNA)
XP_996957 (protein)
Location Chr 17: 7.43 - 7.43 Mb Chr 11: 69.47 - 69.48 Mb
Pubmed search [1] [2]

Mannose-P-dolichol utilization defect 1, also known as MPDU1, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: MPDU1 mannose-P-dolichol utilization defect 1.

[edit] Further reading

  • 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. PMID 8125298. 
  • Ware FE, Lehrman MA (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. PMID 8663248. 
  • 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. PMID 9373149. 
  • Mao M, Fu G, Wu JS, et al. (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. PMID 9653160. 
  • 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. 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. 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. PMID 11733556. 
  • Schenk B, Imbach T, Frank CG, et al. (2002). "MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.". J. Clin. Invest. 108 (11): 1687-95. PMID 11733564. 
  • 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. doi:10.1073/pnas.242603899. 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. 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. 
  • Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry.". Mol. Syst. Biol. 3: 89. doi:10.1038/msb4100134. PMID 17353931. 
 This article on a gene on chromosome 17 is a stub. You can help Wikipedia by expanding it.