| Gene Symbol | GOLGA8FTLDFET |
| Function | is a spectrum of neurodegenerative diseases characterized by abnormal protein aggregates containing FET family proteins (FUS), TAF15, and EWS. |
| Primary Expression | neuronal tissues and is localized to the Golgi apparatus, where it plays a role in protein sorting and trafficking |
| Subcellular Localization | the Golgi apparatus, where it plays a role in protein sorting and trafficking |
| GeneCards | GOLGA8FTLDFET |
| Human Protein Atlas | GOLGA8FTLDFET |
| Gene | GOLGA8 (GOLGA8A/GOLGA8B) |
| Variant | CT dinucleotide repeat expansion in intron |
| Statistical Strength | p = 5.8 × 10⁻²¹, making this one of the strongest genetic associations for a sporadic neurodegenerative disease[@rosa2026] |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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