PRECSIT
gene geneOn this page
Summary
PRECSIT (p53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript, HGNC:27492) is a long non-coding RNA gene on chromosome 13q34.
At a glance
- Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:27492 |
| Approved symbol | PRECSIT |
| Name | p53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript |
| Location | 13q34 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000255874 |
| Ensembl biotype | lncRNA |
| Entrez | 283487 |
| RNAcentral | URS00007599F5 — lncRNA, 6322 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 11 — 11 lncRNA
ENST00000538077, ENST00000693706, ENST00000749866, ENST00000749867, ENST00000749868, ENST00000749869, ENST00000749870, ENST00000749871, ENST00000749872, ENST00000749873, ENST00000749874
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000538077 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00004093800 | 110863987 | 110870454 |
Expression profiles
Bgee: expression breadth ubiquitous, 119 present calls, max score 86.32.
FANTOM5 (CAGE): breadth broad, TPM avg 2.3401 / max 94.2954, expressed in 733 samples.
FANTOM5 promoters (5 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 138272 | 1.6967 | 623 |
| 138271 | 0.3376 | 140 |
| 138273 | 0.1585 | 77 |
| 138269 | 0.1172 | 43 |
| 138270 | 0.0301 | 14 |
Top tissues by expression
119 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| skeletal muscle tissue | UBERON:0001134 | 86.32 | gold quality |
| gastrocnemius | UBERON:0001388 | 84.16 | gold quality |
| muscle of leg | UBERON:0001383 | 84.05 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 83.10 | gold quality |
| placenta | UBERON:0001987 | 69.07 | gold quality |
| calcaneal tendon | UBERON:0003701 | 66.54 | gold quality |
| endometrium | UBERON:0001295 | 65.21 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 64.42 | gold quality |
| thoracic aorta | UBERON:0001515 | 63.74 | gold quality |
| ascending aorta | UBERON:0001496 | 63.45 | gold quality |
| stromal cell of endometrium | CL:0002255 | 62.25 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 59.69 | gold quality |
| apex of heart | UBERON:0002098 | 59.52 | gold quality |
| ventricular zone | UBERON:0003053 | 59.44 | gold quality |
| popliteal artery | UBERON:0002250 | 58.61 | gold quality |
| tibial artery | UBERON:0007610 | 58.58 | gold quality |
| islet of Langerhans | UBERON:0000006 | 58.37 | gold quality |
| right coronary artery | UBERON:0001625 | 58.02 | gold quality |
| mucosa of stomach | UBERON:0001199 | 57.61 | gold quality |
| left coronary artery | UBERON:0001626 | 57.27 | gold quality |
| cortical plate | UBERON:0005343 | 57.24 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 56.83 | gold quality |
| gall bladder | UBERON:0002110 | 56.65 | gold quality |
| ganglionic eminence | UBERON:0004023 | 55.95 | silver quality |
| adipose tissue | UBERON:0001013 | 55.91 | gold quality |
| myometrium | UBERON:0001296 | 55.52 | gold quality |
| body of uterus | UBERON:0009853 | 55.48 | gold quality |
| fallopian tube | UBERON:0003889 | 55.30 | gold quality |
| heart left ventricle | UBERON:0002084 | 54.75 | gold quality |
| ectocervix | UBERON:0012249 | 54.73 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.65 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 10)
- We found that linc00346 was upregulated in bladder cancer tissues compared to normal tissues. Knockdown of linc00346 inhibited bladder cancer cell proliferation and migration, induced cell cycle arrest and cell apoptosis. CONCLUSION: Our study demonstrates that linc00346 could be a potential oncogene and a therapeutic target in bladder cancer. (PMID:28705739)
- The interference in LINC 00346 expression could inhibit the in vivo tumorigenic ability of tumor cells through regulating the Janus kinase/signal transducer and activator of transcription 3 (JAK-STAT3) signaling pathway. (PMID:29228425)
- LINC00346 shows the ability to promote pancreatic cancer growth and gemcitabine resistance, which is in part mediated by antagonization of miR-188-3p and induction of BRD4. Targeting LINC00346 may improve gemcitabine-based therapeutic efficacy. (PMID:30728036)
- LINC00346 promotes hepatocellular carcinoma progression via activating the JAK-STAT3 signaling pathway. (PMID:31478228)
- A positive feedback loop involving the LINC00346/beta-catenin/MYC axis promotes hepatocellular carcinoma development. (PMID:31691159)
- High PRECSIT expression promotes Progression of Cutaneous Squamous Cell Carcinoma via STAT3 Signaling. (PMID:31837949)
- Long non-coding RNA LINC00346 regulates proliferation and apoptosis by targeting miR-128-3p/SZRD1 axis in glioma. (PMID:33015801)
- Upregulation of VDR-associated lncRNAs in Schizophrenia. (PMID:34499334)
- Aberrant expression of LINC00346 regulates cell migration and proliferation via competitively binding to miRNA-148a-3p/Dnmt1 in Hirschsprung’s disease. (PMID:35836014)
- A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma. (PMID:36311792)
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.