Property Summary

NCBI Gene PubMed Count 10
PubMed Score 8.82
PubTator Score 8.69

Knowledge Summary


No data available


  Differential Expression (2)

Disease log2 FC p
malignant mesothelioma 1.100 9.5e-06
psoriasis 1.300 1.2e-03

 GO Function (1)

Protein-protein Interaction (7)

Gene RIF (1)

23109149 We describe a new congenital disorders of glycosylation, due to a deficiency of DPM2

AA Sequence

YVMLKTKRVTKKAQ                                                             71 - 84

Text Mined References (12)

PMID Year Title
23109149 2012 DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
19054851 2008 Human protein factory for converting the transcriptome into an in vitro-expressed proteome,.
16280320 2006 DPM1, the catalytic subunit of dolichol-phosphate mannose synthase, is tethered to and stabilized on the endoplasmic reticulum membrane by DPM3.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
15164053 2004 DNA sequence and analysis of human chromosome 9.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
11591653 2001 Protein-protein interaction panel using mouse full-length cDNAs.
11102867 2000 Dissecting and manipulating the pathway for glycosylphos-phatidylinositol-anchor biosynthesis.
10944123 2000 Initial enzyme for glycosylphosphatidylinositol biosynthesis requires PIG-P and is regulated by DPM2.
10835346 2000 Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3.
9724629 1998 DPM2 regulates biosynthesis of dolichol phosphate-mannose in mammalian cells: correct subcellular localization and stabilization of DPM1, and binding of dolichol phosphate.
8617505 1996 The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression.