Details
| Type | Protein Coding |
| Official Symbol | SQSTM1 |
| Official Name | sequestosome 1 [Source:NCBI gene (formerly Entrezgene);Acc:8878] |
| Ensembl ID | ENSG00000284099 |
| Bio databases IDs | |
| Aliases | sequestosome 1 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the SQSTM1 gene in human plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
- MYOPATHY DISTAL WITH RIMMED VACUOLES
- NEURODEGENERATION WITH ATAXIA DYSTONIA AND GAZE PALSY CHILDHOOD-ONSET
- PAGET DISEASE OF BONE 3