NCBI Description of REEP1
|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.|
Community Annotation of REEP1 Add / Edit REEP1: Annotations
No community annotations yet for REEP1.
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