{"symbol":"REEP1","synonyms":["SPG31","HMN5B","C2ORF23","Yip2a"],"name":"receptor accessory protein 1","description":"This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]","ncbiEntrezGeneId":65055,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/65055","proteins":[{"symbol":"REEP1_HUMAN","href":"/api/1.0/protein/REEP1_HUMAN"}],"hgncRootFamilies":[{"name":"Receptor accessory proteins (REEP)","href":"/api/1.0/gene_family/Receptor+accessory+proteins+%28REEP%29"}]}