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Official Full Name: receptor accessory protein 1
Also known as: DSMA6; HMN5B; SPG31; Yip2a; C2orf23
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.