| Gene Symbol | RTN4IP1 |
| Entrez Gene ID | 84816 |
| Full Name | reticulon 4 interacting protein 1 |
| Synonyms | NIMP,OPA10 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(Human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | Optic atrophy 10 with or without ataxia, mental retardation, and seizures, 616732 (3) |

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