MPDU1

Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.^[5][6][7][8]

MPDU1
Identifiers
Aliases	MPDU1, CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, mannose-P-dolichol utilization defect 1, SLC66A5
External IDs	OMIM: 604041; MGI: 1346040; HomoloGene: 3581; GeneCards: MPDU1; OMA:MPDU1 - orthologs
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17p13.1 Start 7,583,529 bp[1] End 7,592,789 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11 B3|11 42.86 cM Start 69,547,523 bp[2] End 69,553,468 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in rectum mucosa of transverse colon islet of Langerhans right lobe of liver right adrenal cortex left adrenal gland left adrenal cortex granulocyte gallbladder body of stomach Top expressed in yolk sac neural layer of retina lip right kidney morula morula granulocyte ventricular zone ankle joint duodenum More reference expression data BioGPS More reference expression data
Gene ontology Molecular function protein binding Cellular component integral component of membrane extracellular exosome endoplasmic reticulum membrane membrane mitochondrion endoplasmic reticulum Biological process 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

See also

• Dolichol monophosphate mannose
• Congenital disorder of glycosylation