| ID | Sequence | Length | GC content |
|---|---|---|---|
| GGAGAGAUCAGCCGCCCAGCCAGGAGUUAAGCUGAGGUCGUCUGAGCCC… | 1780 nt | 0.5489 | |
| GGAGAGAUCAGCCGCCCAGCCAGGAGUUAAGCUGAGGUCGUCUGAGCCC… | 1653 nt | 0.5481 | |
| GGAGAGAUCAGCCGCCCAGCCAGGAGUUAAGCUGAGGUCGUCUGAGCCC… | 1363 nt | 0.5282 | |
| GGAGAGAUCAGCCGCCCAGCCAGGAGUUAAGCUGAGGUCGUCUGAGCCC… | 1626 nt | 0.5474 |
This gene encodes a member of the interferon regulatory factor (IRF) family, a group of transcription factors with diverse roles, including virus-mediated activation of interferon, and modulation of cell growth, differentiation, apoptosis, and immune system activity. Members of the IRF family are characterized by a conserved N-terminal DNA-binding domain containing tryptophan (W) repeats. Mutations in this gene result in Immunodeficiency 65. [provided by RefSeq, Jul 2020]
A study in humans and mice demonstrated that the IRF9 was identified as a diagnostic and prognostic hub gene in sepsis [Sun et al. DOI:10.3389/fgene.2024.1389630].