{"symbol":"BLOC1S6","synonyms":["PLDN","HPS9","PALLID","BLOS6"],"name":"biogenesis of lysosomal organelles complex-1, subunit 6, pallidin","description":"The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome. [provided by RefSeq, Aug 2015]","ncbiEntrezGeneId":26258,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/26258","proteins":[{"symbol":"BL1S6_HUMAN","href":"/api/1.0/protein/BL1S6_HUMAN"}],"hgncRootFamilies":[{"name":"Biogenesis of lysosomal organelles complex-1 subunits (BLOC1S)","href":"/api/1.0/gene_family/Biogenesis+of+lysosomal+organelles+complex-1+subunits+%28BLOC1S%29"}]}