DPM3

From Wikipedia, the free encyclopedia
Dolichyl-phosphate mannosyltransferase polypeptide 3
Identifiers
SymbolsDPM3; CDG1O
External IDsOMIM: 605951 MGI: 1915813 HomoloGene: 17810 ChEMBL: 3410 GeneCards: DPM3 Gene
EC number2.4.1.83
Orthologs
SpeciesHumanMouse
Entrez5434468563
EnsemblENSG00000179085ENSMUSG00000042737
UniProtQ9P2X0Q9D1Q4
RefSeq (mRNA)NM_018973NM_026767
RefSeq (protein)NP_061846NP_081043
Location (UCSC)Chr 1:
155.11 – 155.11 Mb
Chr 3:
89.26 – 89.27 Mb
PubMed search

dolichyl-phosphate mannosyltransferase polypeptide 3, also known as DPM3, is a human gene.[1][2]

Function

Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. The protein encoded by this gene is a subunit of dolichyl-phosphate mannosyltransferase and acts as a stabilizer subunit of the dolichyl-phosphate mannosyltransferase complex.[1]

Clinical significance

Mutations in this gene are associated with congenital disorder of glycosylation type 1O.[3]

References

  1. 1.0 1.1 "Entrez Gene: dolichyl-phosphate mannosyltransferase polypeptide 3". 
  2. Maeda Y, Tanaka S, Hino J, Kangawa K, Kinoshita T (June 2000). "Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3". EMBO J. 19 (11): 2475–82. doi:10.1093/emboj/19.11.2475. PMC 212771. PMID 10835346. 
  3. Haeuptle MA, Hennet T (December 2009). "Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol-linked oligosaccharides". Hum. Mutat. 30 (12): 1628–41. doi:10.1002/humu.21126. PMID 19862844. 

Further reading

External links


This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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