| Gene Symbol | UBQLN2 |
| Full Name | Ubiquilin 2 |
| Chromosome | Xp11.21 |
| Protein Family | Ubiquilin family |
| Function | Contains disease-causing mutations (P497H, P506T) |
| Primary Expression | Motor cortex, Spinal cord, Hippocampus |
| Subcellular Localization | Cytoplasm, nucleus |
| Molecular Weight | 66 kDa |
| Amino Acids | 600 aa |
| Exons | 11 |
| Pathways | Protein Degradation |
| UniProt ID | Q9R0R5 |
| NCBI Gene ID | 29978 |
| Ensembl ID | ENSG00000188021 |
| OMIM | 300264 |
| GeneCards | UBQLN2 |
| Human Protein Atlas | UBQLN2 |
| Associated Diseases | ALS, Amyotrophic Lateral Sclerosis, FTLD, Ms, NEURODEGENERATION |
| Interactions | HSP70, UNC5B, TIA1, HSPA1B, TDP-43, VAPB |
| KG Connections | 189 knowledge graph edges |
| Databases | GeneCardsHPASTRING |