LSINCT5
gene geneOn this page
Summary
LSINCT5 (long stress-induced non-coding transcript 5, HGNC:37824) is a long non-coding RNA gene on chromosome 5p15.33.
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:37824 |
| Approved symbol | LSINCT5 |
| Name | long stress-induced non-coding transcript 5 |
| Location | 5p15.33 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000281560 |
| Ensembl biotype | lncRNA |
| OMIM | 615764 |
| Entrez | 101234261 |
| RNAcentral | URS000020D25D — lncRNA, 2647 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 lncRNA
ENST00000626215
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000626215 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003773368 | 2712591 | 2715237 |
Expression profiles
Bgee: expression breadth broad, 34 present calls, max score 57.88.
Top tissues by expression
34 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| minor salivary gland | UBERON:0001830 | 57.88 | gold quality |
| saliva-secreting gland | UBERON:0001044 | 57.80 | gold quality |
| blood | UBERON:0000178 | 53.74 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 48.42 | gold quality |
| heart left ventricle | UBERON:0002084 | 46.76 | silver quality |
| islet of Langerhans | UBERON:0000006 | 46.72 | gold quality |
| fundus of stomach | UBERON:0001160 | 46.71 | gold quality |
| heart | UBERON:0000948 | 45.89 | silver quality |
| body of stomach | UBERON:0001161 | 44.93 | gold quality |
| zone of skin | UBERON:0000014 | 43.91 | silver quality |
| skin of abdomen | UBERON:0001416 | 43.90 | silver quality |
| skin of leg | UBERON:0001511 | 43.84 | silver quality |
| right lung | UBERON:0002167 | 43.73 | silver quality |
| placenta | UBERON:0001987 | 43.17 | silver quality |
| lung | UBERON:0002048 | 42.29 | silver quality |
| metanephros cortex | UBERON:0010533 | 41.97 | silver quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 41.56 | silver quality |
| gastrocnemius | UBERON:0001388 | 41.53 | silver quality |
| tibial artery | UBERON:0007610 | 41.47 | silver quality |
| tibial nerve | UBERON:0001323 | 41.44 | gold quality |
| upper lobe of left lung | UBERON:0008952 | 41.15 | silver quality |
| subcutaneous adipose tissue | UBERON:0002190 | 40.70 | silver quality |
| colon | UBERON:0001155 | 40.69 | silver quality |
| Ammon’s horn | UBERON:0001954 | 40.41 | silver quality |
| lower esophagus muscularis layer | UBERON:0035833 | 40.26 | silver quality |
| esophagus mucosa | UBERON:0002469 | 40.14 | silver quality |
| adult mammalian kidney | UBERON:0000082 | 39.77 | silver quality |
| prostate gland | UBERON:0002367 | 38.87 | silver quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 37.95 | silver quality |
| hypothalamus | UBERON:0001898 | 37.79 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 2.61 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 15)
- The ectopic expression of LSINCT5 in gastrointestinal cancer cell lines resulted in an increase in cellular proliferation; conversely, knock down of LSINCT5 significantly inhibited proliferation. (PMID:25526476)
- Circulating CUDR, LSINCT-5 and PTENP1 were identified as potential diagnostic markers for gastric cancer diagnosis. (PMID:25694351)
- high expression levels of BNP promote the apoptosis of myocardial cells through the lncRNA LSINCT5 mediator. (PMID:26323562)
- lncRNA long stress-induced noncoding transcript 5 (LSINCT5) is significantly upregulated in human bladder cancer cell lines and tumor specimens. Mechanistic investigations showed that LSINCT5 could physically interact with NCYM, a de novo gene product from the MYCN cis-antisense RNA and inhibit GSK3beta activity leading to enhanced Wnt/beta-catenin signaling activation and epithelial mesenchymal transition (EMT). (PMID:29772237)
- The expression levels of LSINCT5 was related to the body mass index in women. (PMID:29785740)
- LSINCT5 may possibly contribute to non-small cell lung cancer tumorigenesis by stabilizing the oncogenic factor of HMGA2. (PMID:29883241)
- LSINCT5 interacted with EZH2 to suppress the expression of APC, a negative regulator of the Wnt/beta-catenin pathway. (PMID:30420287)
- LSINCT5 could bind to HMGA2 and decrease proteasome-mediated HMGA2 degradation leading to EMT activation. LSINCT5 also served as a competing endogenous RNA (ceRNA) for miR-4516, resulting in increased STAT3/BclxL expression and attenuated apoptosis. (PMID:30472720)
- study suggests that LSINCT5 exerts oncogenic function in osteosarcoma cells, and may be a potential predictor for clinical outcome in osteosarcoma patients. (PMID:30967495)
- Down-regulation of LSINCT5 represses glioma cells growth and metastasis in vitro likely through targeting miR-451 and thereby inhibiting Rac1-regulated PI3K/AKT, Wnt/beta-catenin and NF-kappaB pathways (PMID:31213092)
- Long noncoding RNA LSINCT5 is upregulated and promotes the progression of esophageal squamous cell carcinoma. (PMID:31298370)
- Effect of long non-coding RNA long stress-induced noncoding transcript 5 on erlotinib resistance to lung cancer cells and the underlying mechanisms.", trans “RNA5. (PMID:33053528)
- LncRNA LSINCT5 drives proliferation and migration of oral squamous cell carcinoma through the miRNA-185-5p/ZNF703 axis. (PMID:33721442)
- LncRNA LSINCT5/miR-222 regulates myocardial ischemiareperfusion injury through PI3K/AKT pathway. (PMID:34184201)
- LSINCT5: A Novel lncRNA in Cancers. (PMID:36734894)
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.