Details
| Type | Protein Coding |
| Official Symbol | SMARCB1 |
| Official Name | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 [Source:HGNC Symbol;Acc:HGNC:11103] |
| Ensembl ID | ENSG00000275837 |
| Bio databases IDs | |
| Aliases | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the SMARCB1 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
- COFFIN-SIRIS SYNDROME 3
- RHABDOID TUMOR PREDISPOSITION SYNDROME 1
- SCHWANNOMATOSIS 1
- EHMT1-like SYNDROME
- Rhabdoid predisposition syndrome 1