Matches in DBpedia 2014 for { <http://dbpedia.org/resource/AP3B1> ?p ?o. }
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- AP3B1 abstract "AP-3 complex subunit beta-1 is a protein that in humans is encoded by the AP3B1 gene.This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2.".
- AP3B1 entrezgene "8546".
- AP3B1 wikiPageExternalLink br.fcgi?book=gene&part=hps.
- AP3B1 wikiPageID "14775013".
- AP3B1 wikiPageRevisionID "590598553".
- AP3B1 hasPhotoCollection AP3B1.
- AP3B1 requireManualInspection "no".
- AP3B1 summaryText "This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2.".
- AP3B1 updateCitations "yes".
- AP3B1 updatePage "yes".
- AP3B1 updateProteinBox "yes".
- AP3B1 updateSummary "yes".
- AP3B1 type Biomolecule.
- AP3B1 type Protein.
- AP3B1 type BiologicalObject.
- AP3B1 comment "AP-3 complex subunit beta-1 is a protein that in humans is encoded by the AP3B1 gene.This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2.".
- AP3B1 label "AP3B1".
- AP3B1 sameAs m.03gxlr7.
- AP3B1 sameAs Q4653197.
- AP3B1 sameAs Q4653197.
- AP3B1 sameAs AP3B1.
- AP3B1 wasDerivedFrom AP3B1?oldid=590598553.
- AP3B1 isPrimaryTopicOf AP3B1.