| Gene Symbol | ANXA11 |
| Aliases | ANXA11PROTEIN |
| Chromosome | 10q22.3 |
| Function | N-terminal low-complexity domain (LCD, residues 1–188): An intrinsically disordered region enriched in glycine and proline residues. |
| Primary Expression | Motor neurons, Cortex, Hippocampus, Spinal cord |
| Subcellular Localization | </th><td>Cytoplasm; nucleus; plasma membrane; cytoskeleton</td></tr> |
| Amino Acids | 505 aa |
| UniProt ID | P50995 |
| Ensembl ID | ENSG00000122359 |
| OMIM | 602572 |
| GeneCards | ANXA11 |
| Human Protein Atlas | ANXA11 |
| Associated Diseases | Alzheimer's disease, FTLD-TDP, NTDs, amyotrophic lateral sclerosis, frontotemporal dementia, neurodegeneration |
| Interactions | TDP-43, TARDBP |
| KG Connections | 62 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |