MPDU1, mannose-P-dolichol utilization defect 1

MPDU1, mannose-P-dolichol utilization defect 1

• This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]

• Gene Synonyms (mannose-P-dolichol utilization defect 1 protein, HBeAg-binding protein 2 binding protein A, suppressor of Lec15 and Lec35 glycosylation mutation homolog, CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, SLC66A5,)
• NCBI Gene ID: 9526
• Species: Homo sapiens (Human)
• UNIPROT ID#>>J3QW43
  UNIPROT ID#>>B4DLH7
  UNIPROT ID#>>O75352
  UNIPROT ID#>>A0A0S2Z4W8
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

mannose-P-dolichol utilization defect 1 interacts with:

• glutamine rich 2
  LSM1 homolog, mRNA degradation associated
  mannosidase beta like
  mortality factor 4 like 2
  nuclear RNA export factor 1
  phosphomevalonate kinase
  synoviolin 1

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