MPDU1

Mannose-P-dolichol utilization defect 1
Identifiers
Symbols MPDU1 ; CDGIF; HBEBP2BPA; Lec35; My008; PP3958; PQLC5; SL15
External IDs OMIM: 604041 MGI: 1346040 HomoloGene: 3581 GeneCards: MPDU1 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 9526 24070
Ensembl ENSG00000129255 ENSMUSG00000018761
UniProt O75352 Q8R0J2
RefSeq (mRNA) NM_004870 NM_001301710
RefSeq (protein) NP_004861 NP_001288639
Location (UCSC) Chr 17:
7.58 – 7.59 Mb
Chr 11:
69.66 – 69.66 Mb
PubMed search

Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.[1][2][3][4]

See also

References

  1. 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.
  2. 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. doi:10.1073/pnas.95.14.8175. PMC 20949. PMID 9653160.
  3. 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.
  4. "Entrez Gene: MPDU1 mannose-P-dolichol utilization defect 1".

Further reading

External links


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