| ID | Sequence | Length | GC content |
|---|---|---|---|
| CCUUCUCUCUUCUUAGAGACAACAGGUGGCUGGGGCCUCAGUGCCCAGA… | 843 nt | 0.5848 | |
| AUUUAGGCGGUGACAGACAGCAUCCGCAGUCAAUAGGAAGAGCUGAAGA… | 847 nt | 0.5809 | |
| GACUCCUUGCUUCUUUCCAGCCGGAGCCGCUGCCUUGCCCCCCGGAGAC… | 657 nt | 0.5784 |
Predicted to enable calcium ion binding activity. Predicted to be a structural constituent of muscle. Involved in muscle contraction. Located in lysosomal membrane. Implicated in distal arthrogryposis type 1C. [provided by Alliance of Genome Resources, Jul 2025]
A study in humans identified the MYL11 as a gene marker highly expressed in cavernosal trabecular smooth muscle cells (CCSMC) within the corpus cavernosum, with its expression being especially elevated in patients with erectile dysfunction [Zhao et al. DOI:10.1038/s41467-022-31950-9]. In forensic science, targeted massively parallel sequencing assays have utilized the MYL11 as an mRNA marker for the specific identification of skeletal muscle tissue in human samples [Haas et al. DOI:10.1016/j.fsigen.2021.102486]. A study in mice demonstrated that the MYL11 is a protein-coding gene associated with sarcomeric function and is linked to ChIP-clusters enriched in down-regulated long non-coding RNAs following myocardial infarction [Ounzain et al. DOI:10.1093/eurheartj/ehu180]. In rats, RNA sequencing of cardiac fibroblasts across developmental ages identified the MYL11 as an RNA marker for cardiac development/function, showing it was significantly downregulated in adult cardiac fibroblasts compared to neonatal and fetal groups and was associated with the neonatal/fetal cluster in principal component analysis [Perreault et al. DOI:10.1152/physiolgenomics.00074.2021].