| Gene Symbol | FIGN |
| Aliases | FIGNPROTEIN |
| Chromosome | 4. |
| Function | FIGN is a AAA+ ATPase with microtubule-severing activity. |
| Primary Expression | various brain regions: |
| Subcellular Localization | . The AAA+ ATPase domains enable formation of ring-like oligomeric structures believed necessary for substrate engagemen |
| Molecular Weight | 49 kDa |
| Amino Acids | 425 aa |
| UniProt ID | Q8N8Y0 |
| Ensembl ID | ENSG00000101940 |
| GeneCards | FIGN |
| Human Protein Atlas | FIGN |
| Spastin (SPAST) | Another AAA+ ATPase microtubule-severing protein mutated in HSP |
| Katanin | Related microtubule-severing protein family |
| Hereditary Spastic Paraplegia | Primary disease associated with FIGN mutations |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsNCBI GeneHPASTRING |
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