| Entrez Gene ID | 3925 |
|---|---|
| Official Gene Symbol | STMN1 (GeneCards) |
| Full name | stathmin 1 |
| Location | 1p36.11 |
| Other ids | Vega : OTTHUMG00000007389 MIM : 151442 HGNC : HGNC:6510 Ensembl : ENSG00000117632 |
| Other names | Lag, SMN, OP18, PP17, PP19, PR22, LAP18, C1orf215 |
| Summary | This gene belongs to the stathmin family of genes. It encodes a ubiquitous cytosolic phosphoprotein proposed to function as an intracellular relay integrating regulatory signals of the cellular environment. The encoded protein is involved in the regulation of the microtubule filament system by destabilizing microtubules. It prevents assembly and promotes disassembly of microtubules. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009] |
Found 4 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 1546 | 3925 | STMN1 | 1 | 26228141 | 26228141 | Autism Spectrum Disorders | NextSeq500 v2 |
| 1547 | 3925 | STMN1 | 1 | 26228141 | 26228141 | Autism Spectrum Disorders | NextSeq500 v2 |
| 24330 | 3925 | STMN1 | 1 | 26263087 | 26263087 | Asymptomatic | NextSeq500 v2 Single cell Sequencing Cell cloning |
| 29705 | 3925 | STMN1 | 1 | 26228141 | 26228141 | Autism Spectrum Disorders | NextSeq500 v2 Single cell Sequencing Cell cloning NextSeq500 |