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- DPAGT1 abstract "UDP-N-acetylglucosamine—dolichyl-phosphate N-acetylglucosaminephosphotransferase is an enzyme that in humans is encoded by the DPAGT1 gene.Mutations in DPAGT1 cause myasthenia . The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway (also see Genetic pathway) for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme. Alternatively spliced transcript variants encoding different isoforms have been identified.".
- DPAGT1 entrezgene "1798".
- DPAGT1 wikiPageExternalLink NBK1332.
- DPAGT1 wikiPageID "14817121".
- DPAGT1 wikiPageLength "7320".
- DPAGT1 wikiPageOutDegree "17".
- DPAGT1 wikiPageRevisionID "678196703".
- DPAGT1 wikiPageWikiLink Biosynthesis.
- DPAGT1 wikiPageWikiLink Catalysis.
- DPAGT1 wikiPageWikiLink Catalyzes.
- DPAGT1 wikiPageWikiLink Congenital_disorder_of_glycosylation.
- DPAGT1 wikiPageWikiLink Dolichol.
- DPAGT1 wikiPageWikiLink Endoplasmic_reticulum.
- DPAGT1 wikiPageWikiLink Enzyme.
- DPAGT1 wikiPageWikiLink Gene.
- DPAGT1 wikiPageWikiLink Gene_regulatory_network.
- DPAGT1 wikiPageWikiLink Genetic_pathway.
- DPAGT1 wikiPageWikiLink Glycoprotein.
- DPAGT1 wikiPageWikiLink Glycosyltransferase.
- DPAGT1 wikiPageWikiLink Human.
- DPAGT1 wikiPageWikiLink Humans.
- DPAGT1 wikiPageWikiLink Membrane_protein.
- DPAGT1 wikiPageWikiLink Metabolic_pathway.
- DPAGT1 wikiPageWikiLink Mutation.
- DPAGT1 wikiPageWikiLink Oligosaccharide.
- DPAGT1 wikiPageWikiLink Protein.
- DPAGT1 wikiPageWikiLink Transcription_(genetics).
- DPAGT1 wikiPageWikiLinkText "DPAGT1".
- DPAGT1 hasPhotoCollection DPAGT1.
- DPAGT1 label "myasthenia".
- DPAGT1 requireManualInspection "no".
- DPAGT1 summaryText "The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme. Alternatively spliced transcript variants encoding different isoforms have been identified.".
- DPAGT1 target "muscle weakness".
- DPAGT1 type "genetic_defect_results_in_disease".
- DPAGT1 updateCitations "yes".
- DPAGT1 updatePage "yes".
- DPAGT1 updateProteinBox "yes".
- DPAGT1 updateSummary "yes".
- DPAGT1 wikiPageUsesTemplate Template:Cite_journal.
- DPAGT1 wikiPageUsesTemplate Template:Gene-11-stub.
- DPAGT1 wikiPageUsesTemplate Template:PBB.
- DPAGT1 wikiPageUsesTemplate Template:PBB_Controls.
- DPAGT1 wikiPageUsesTemplate Template:PBB_Further_reading.
- DPAGT1 wikiPageUsesTemplate Template:PBB_Summary.
- DPAGT1 wikiPageUsesTemplate Template:Refbegin.
- DPAGT1 wikiPageUsesTemplate Template:Refend.
- DPAGT1 wikiPageUsesTemplate Template:Reflist.
- DPAGT1 wikiPageUsesTemplate Template:SWL.
- DPAGT1 wikiPageUsesTemplate Template:Technical.
- DPAGT1 hypernym Enzyme.
- DPAGT1 type Article.
- DPAGT1 type Biomolecule.
- DPAGT1 type Protein.
- DPAGT1 type Article.
- DPAGT1 type Thing.
- DPAGT1 type Q206229.
- DPAGT1 type Q8054.
- DPAGT1 comment "UDP-N-acetylglucosamine—dolichyl-phosphate N-acetylglucosaminephosphotransferase is an enzyme that in humans is encoded by the DPAGT1 gene.Mutations in DPAGT1 cause myasthenia . The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway (also see Genetic pathway) for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4.".
- DPAGT1 label "DPAGT1".
- DPAGT1 sameAs m.03gyy_d.
- DPAGT1 sameAs Q5205915.
- DPAGT1 sameAs Q5205915.
- DPAGT1 wasDerivedFrom DPAGT1?oldid=678196703.
- DPAGT1 isPrimaryTopicOf DPAGT1.