MPDU1
Sign in to saveAlso known as CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, mannose-P-dolichol utilization defect 1
Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.
Gene data
MPDU1- Name
- mannose-P-dolichol utilization defect 1
- Type
- protein-coding
- Aliases
- CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, SLC66A5
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].
via MyGene.info
Gene · Ensembl
mannose-P-dolichol utilization defect 1
- Symbol
- MPDU1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:7,583,214-7,594,419
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 3581
- exact match
- identifiers.org/ncbigene/9526
- genomic end
- 7496107
- genomic start
- 7486847
- cytogenetic location
- 17p13.1
Sources (4)
via Wikidata · CC0
~1 min read
Article
4 sectionsContents
- See also
- References
- Further reading
- External links
Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.
==See also== Dolichol monophosphate mannose Congenital disorder of glycosylation