Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/DGCR6> ?p ?o }
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- DGCR6 abstract "Protein DGCR6 is a protein that in humans is encoded by the DGCR6 gene.DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. This gene product shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the human laminin gamma-1 chain, which upon polymerization with alpha- and beta-chains forms the laminin molecule. Laminin binds to cells through interaction with a receptor and has functions in cell attachment, migration, and tissue organization during development. This gene could be a candidate for involvement in the DiGeorge syndrome pathology by playing a role in neural crest cell migration into the third and fourth pharyngeal pouches, the structures from which derive the organs affected in DiGeorge syndrome.".
- DGCR6 entrezgene "8214".
- DGCR6 wikiPageID "15416906".
- DGCR6 wikiPageLength "4736".
- DGCR6 wikiPageOutDegree "2".
- DGCR6 wikiPageRevisionID "661000762".
- DGCR6 wikiPageWikiLink Gene.
- DGCR6 wikiPageWikiLink Protein.
- DGCR6 wikiPageWikiLinkText "DGCR6".
- DGCR6 requireManualInspection "no".
- DGCR6 summaryText "DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. This gene product shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the human laminin gamma-1 chain, which upon polymerization with alpha- and beta-chains forms the laminin molecule. Laminin binds to cells through interaction with a receptor and has functions in cell attachment, migration, and tissue organization during development. This gene could be a candidate for involvement in the DiGeorge syndrome pathology by playing a role in neural crest cell migration into the third and fourth pharyngeal pouches, the structures from which derive the organs affected in DiGeorge syndrome.".
- DGCR6 updateCitations "yes".
- DGCR6 updatePage "yes".
- DGCR6 updateProteinBox "yes".
- DGCR6 updateSummary "yes".
- DGCR6 wikiPageUsesTemplate Template:Cite_journal.
- DGCR6 wikiPageUsesTemplate Template:Gene-22-stub.
- DGCR6 wikiPageUsesTemplate Template:Orphan.
- DGCR6 wikiPageUsesTemplate Template:PBB.
- DGCR6 wikiPageUsesTemplate Template:PBB_Controls.
- DGCR6 wikiPageUsesTemplate Template:PBB_Further_reading.
- DGCR6 wikiPageUsesTemplate Template:PBB_Summary.
- DGCR6 wikiPageUsesTemplate Template:Refbegin.
- DGCR6 wikiPageUsesTemplate Template:Refend.
- DGCR6 wikiPageUsesTemplate Template:Reflist.
- DGCR6 hypernym Protein.
- DGCR6 type Biomolecule.
- DGCR6 type Protein.
- DGCR6 type Thing.
- DGCR6 type Q206229.
- DGCR6 type Q8054.
- DGCR6 comment "Protein DGCR6 is a protein that in humans is encoded by the DGCR6 gene.DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. This gene product shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the human laminin gamma-1 chain, which upon polymerization with alpha- and beta-chains forms the laminin molecule.".
- DGCR6 label "DGCR6".
- DGCR6 sameAs Q18032767.
- DGCR6 sameAs m.03m7yq2.
- DGCR6 sameAs Q18032767.
- DGCR6 wasDerivedFrom DGCR6?oldid=661000762.
- DGCR6 isPrimaryTopicOf DGCR6.