| Gene Symbol | AFG3L2 |
| Entrez Gene ID | 10939 |
| Full Name | AFG3 like matrix AAA peptidase subunit 2 |
| Synonyms | SCA28,SPAX5 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | Spinocerebellar ataxia 28, 610246 (3); Spastic ataxia 5, autosomal recessive, 614487 (3) |








































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