{"symbol":"RTN4IP1","synonyms":["OPA10","NIMP"],"name":"reticulon 4 interacting protein 1","description":"This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, cognitive disability, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","ncbiEntrezGeneId":84816,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84816","proteins":[{"symbol":"RT4I1_HUMAN","href":"/api/1.0/protein/RT4I1_HUMAN"}],"hgncRootFamilies":[]}