| ID | Sequence | Length | GC content |
|---|---|---|---|
| XIST:28 | AUAUUUCUUACUCUCUCGGGGCUGGAAGCUUCCUGACUGAAGAUCUCUC… | 9200 nt | 0.4077 |
| XIST:29 | AUAUUUCUUACUCUCUCGGGGCUGGAAGCUUCCUGACUGAAGAUCUCUC… | 5302 nt | 0.4510 |
| XIST:3 | CCUUCAGUUCUUAAAGCGCUGCAAUUCGCUGCUGCAGCCAUAUUUCUUA… | 19280 nt | 0.4121 |
| XIST:30 | AUAUUUCUUACUCUCUCGGGGCUGGAAGCUUCCUGACUGAAGAUCUCUC… | 4313 nt | 0.4572 |
| XIST:31 | AUAUUUCUUACUCUCUCGGGGCUGGAAGCUUCCUGACUGAAGAUCUCUC… | 19236 nt | 0.4119 |
| XIST:32 | AGCAGAAGAUGGAAUUAGACUGAUGACACACUGUCCAGCUACUCAGCGA… | 2865 nt | 0.4325 |
| XIST:33 | CCUACCCCCCUACCCCCCUCUGGUCUGCCCUGCACUGCACUGUUGCCAU… | 16643 nt | 0.4024 |
| XIST:34 | CCUACCCCCCUACCCCCCUCUGGUCUGCCCUGCACUGCACUGUUGCCAU… | 16007 nt | 0.4000 |
| XIST:35 | CCUACCCCCCUACCCCCCUCUGGUCUGCCCUGCACUGCACUGUUGCCAU… | 2492 nt | 0.4185 |
| XIST:36 | AGUGCUCCAGGCCUGCUUGGUGUGGACAUGGUGGUGAGCCGUGGCAAGG… | 11477 nt | 0.4327 |
X inactivation is an early developmental process in mammalian females that transcriptionally silences one of the pair of X chromosomes, thus providing dosage equivalence between males and females. The process is regulated by several factors, including a region of chromosome X called the X inactivation center (XIC). The XIC comprises several non-coding and protein-coding genes, and this gene was the first non-coding gene identified within the XIC. This gene is expressed exclusively from the XIC of the inactive X chromosome, and is essential for the initiation and spread of X-inactivation. The transcript is a spliced RNA. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined. Mutations in the XIST promoter cause familial skewed X inactivation. [provided by RefSeq, Apr 2012]
A study in humans demonstrated that the XIST was identified among transcripts important for predicting multiple organ failure/dysfunction syndrome (MOF/MODS) outcome from blood transcriptome analysis within 24 hours of traumatic injury using an XGBoost machine learning model [Duran et al. DOI:10.1186/s13613-024-01364-5]. A study in humans demonstrated that the XIST was significantly downregulated in peripheral blood mononuclear cells of patients with acute myocardial infarction compared to noncoronary artery controls, as identified by RNA sequencing and validated by quantitative real-time PCR [Zhao et al. DOI:10.1097/MD.0000000000012604].