REEP1, receptor accessory protein 1

REEP1, 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]

• Gene Synonyms (receptor expression-enhancing protein 1, spastic paraplegia 31 protein, C2orf23, HMN5B, SPG31, Yip2a,)
• NCBI Gene ID: 65055
• Species: Homo sapiens (Human)
• UNIPROT ID#>>E7EUF7
  UNIPROT ID#>>Q9H902
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

receptor accessory protein 1 interacts with:

• receptor accessory protein 4
  transmembrane protein 42
  unc-93 homolog B1, TLR signaling regulator

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.