Synonyms:C2orf23, ENTREZ:65055, HGNC:25786, HMN5B, MIM:609139, NM_001164730, NM_001164731, NM_001164732, NM_001371279, NM_001371280, NM_022912, NP_001158202, NP_001158203, NP_001158204, NP_001358208, NP_001358209, NP_075063, REEP1, SPG31, XM_005264504, XM_011533044, XM_011533045, XM_017004725, XM_017004726, XM_017004727, XP_005264561, XP_011531346, XP_011531347, XP_016860214, XP_016860215, XP_016860216, Yip2a, receptor accessory protein 1
Omim:OMIM:609139
Id:ENSG00000068615
Hgnc:HGNC:25786
Description:receptor accessory protein 1
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]