| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGAGUGUGGUCAGGCGGCUCGGACUGAGCAGGACUUUCCUUAUCCCAGU… | 2162 nt | 0.4977 | |
| AGAGUGUGGUCAGGCGGCUCGGACUGAGCAGGACUUUCCUUAUCCCAGU… | 1443 nt | 0.4310 | |
| AGAAGGGGCACUGCUCUGUCCGAGUGCUGCCCUUGGGGCGAGGCGGGCA… | 1505 nt | 0.4385 | |
| AUUGUCUGAAGGGACGGGGCGGUGCCCCAGGGACCAGCGGCUUUAGGAC… | 1606 nt | 0.4620 |
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] CIViC Summary for STMN1 Gene
A study in mice demonstrated that the STMN1 is a hub gene highly expressed 3-days after spinal cord injury, where it is closely related to ferroptosis and immune cell infiltration, and its diagnostic efficacy was confirmed with an AUC of 0.999 [Bao et al. DOI:10.1186/s13018-023-04195-5]. In human skin, the STMN1 was identified as a marker for proliferating basal keratinocytes (Bas-prolif) during wound healing [Liu et al. DOI:10.1016/j.stem.2024.11.013].