dolichol-linked oligosaccharide biosynthetic process
oligosaccharide biosynthetic process
protein folding
transport
Sources:Amigo / QuickGO
Orthologs
Species
Human
Mouse
Entrez
9526
24070
Ensembl
ENSG00000129255
ENSMUSG00000018761
UniProt
O75352
Q9R0Q9
RefSeq (mRNA)
NM_004870 NM_001330073
NM_001301710 NM_001301711 NM_011900
RefSeq (protein)
NP_001317002 NP_004861
n/a
Location (UCSC)
Chr 17: 7.58 – 7.59 Mb
Chr 11: 69.55 – 69.55 Mb
PubMed search
[3]
[4]
Wikidata
View/Edit Human
View/Edit Mouse
Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.[5][6][7][8]
^ 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. 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.
utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene. Dolichol monophosphate mannose Congenital disorder of glycosylation...
Ie; 608799; DPM1 Congenital disorder of glycosylation, type If; 609180; MPDU1 Congenital disorder of glycosylation, type Ig; 607143; ALG12 Congenital...