| ID | Sequence | Length | GC content |
|---|---|---|---|
| NEAT1:2 | CUGACCUGGCUUCAGAACAAGAUGUGGGGCUCCAGGCACCCGGGAGACC… | 1913 nt | 0.5363 |
| NEAT1:20 | AGUGAGCAGCACUGCCCGCCCAGGCAACCUGGAACCAGGGUCGUGCCCC… | 20864 nt | 0.4514 |
| NEAT1:21 | GACAGUGCAGUUUCCAGACCCAGGCCCUGAGCUGAGGGGCCUCAGGGCU… | 26588 nt | 0.4672 |
| NEAT1:22 | GCCUCCCAAAUGUCACCUUGAGCGCUGUCCGCGAUCCCAAAAAGCACUG… | 14927 nt | 0.4364 |
| NEAT1:23 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 1474 nt | 0.5821 |
| NEAT1:24 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 1721 nt | 0.5404 |
| NEAT1:25 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 1952 nt | 0.5446 |
| NEAT1:26 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 6847 nt | 0.4611 |
| NEAT1:27 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 22743 nt | 0.4405 |
| NEAT1:28 | GGAGUUAGCGACAGGGAGGGAUGCGCGCCUGGGUGUAGUUGUGGGGGAG… | 22525 nt | 0.4404 |
This gene produces a long non-coding RNA (lncRNA) transcribed from the multiple endocrine neoplasia locus. This lncRNA is retained in the nucleus where it forms the core structural component of the paraspeckle sub-organelles. It may act as a transcriptional regulator for numerous genes, including some genes involved in cancer progression. [provided by RefSeq, Mar 2015]
A study in human postmortem midbrain specimens from chronic cocaine abusers identified a profile of 32 dysregulated long noncoding RNAs (lncRNAs) using a custom microarray, with differential expression validated by qPCR and in situ hybridization for a subset, including dopamine neuron-specific localization for LINC00162 and TRAF3IP2-AS1 [Bannon et al. DOI:10.1111/jnc.13255]. A review notes that the lncRNA NEAT1 is upregulated in the peripheral blood of Parkinson's disease patients and sponges miR-124 to accelerate pathology, highlighting its role as a biomarker in neurological disorders [Das et al. DOI:10.1080/21655979.2021.2003667]. A review of forensic proteomics literature identifies the NEAT1 as a protein marker for post-mortem interval (PMI) estimation in early PMI skeletal muscle, where it shows degradation products post-mortem [Alex et al. DOI:10.1016/j.scijus.2025.101320].