| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUUUGUGGUGAGAUUCUCUCCCAGGCCACAAGACAUUUCCUGCUCGGAA… | 2267 nt | 0.4089 | |
| AAGAAUUUACCGGCAGGCAGGUCUGGUCCCAGCAGAGGAGACCCAGGGG… | 1472 nt | 0.4633 | |
| AUUUGUGGUGAGAUUCUCUCCCAGGCCACAAGACAUUUCCUGCUCGGAA… | 1374 nt | 0.4374 |
Predicted to enable chromatin binding activity. Predicted to be involved in positive regulation of cold-induced thermogenesis and positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including brown fat cell differentiation; defense response to bacterium; and response to cold. Predicted to be located in azurophil granule lumen and extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
A study in mice demonstrated that the PLAC8 was previously identified with strong classification performance for sepsis and was validated in human cohorts, where its combination with CLU achieved high classification accuracy for distinguishing septic patients from healthy individuals [Zhang et al. DOI:10.1093/jimmun/vkaf140]. In human diagnostic model development, the PLAC8 was mentioned as an existing biomarker developed from microarray data and used for performance comparison against a novel deep learning framework [Zheng et al. DOI:10.1371/journal.pcbi.1012083].