{"symbol":"HPS6","synonyms":["BLOC2S3"],"name":"Hermansky-Pudlak syndrome 6","description":"This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":79803,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/79803","proteins":[{"symbol":"HPS6_HUMAN","href":"/api/1.0/protein/HPS6_HUMAN"}],"hgncRootFamilies":[]}