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REEP1

Official Full Name
receptor accessory protein 1
Organism
Homo sapiens
GeneID
65055
Background
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]
Synonyms
DSMA6; HMN5B; HMNR6; SPG31; Yip2a; HMND12; C2orf23;

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