| Entrez gene ID | | 80208 |
| Official gene symbol | | SPG11 |
| Full name | | spastic paraplegia 11 (autosomal recessive) |
| Aliases | | ,DKFZp762B1512,FLJ21439,KIAA1840, |
| Gene summary | | The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq] |
| Location | | Chromosome: 15 Locus: 15q14 |
| Gene position | | 44955876 - 44854894 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 100983 bp |
| Gene sequence |
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| OMIM ID | | 610844 |