TUSC7
gene geneOn this page
Also known as LINC00902LOC285194
Summary
TUSC7 (tumor suppressor candidate 7, HGNC:27701) is a long non-coding RNA gene on chromosome 3q13.31.
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:27701 |
| Approved symbol | TUSC7 |
| Name | tumor suppressor candidate 7 |
| Location | 3q13.31 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | LINC00902, LOC285194 |
| Ensembl gene | ENSG00000243197 |
| Ensembl biotype | lncRNA |
| OMIM | 616057 |
| Entrez | 285194 |
| RNAcentral | URS00026A1F84 — lncRNA, 2107 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 9 — 9 lncRNA
ENST00000466156, ENST00000466856, ENST00000477539, ENST00000477805, ENST00000496154, ENST00000496242, ENST00000609361, ENST00000660554, ENST00000665622
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000466156 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001862911 | 116712355 | 116712599 |
| ENSE00001895289 | 116716188 | 116716431 |
| ENSE00001929387 | 116714039 | 116714150 |
| ENSE00001941677 | 116709969 | 116710421 |
Expression profiles
Bgee: expression breadth broad, 85 present calls, max score 85.17.
Top tissues by expression
85 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| corpus callosum | UBERON:0002336 | 85.17 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 84.68 | gold quality |
| left testis | UBERON:0004533 | 81.18 | gold quality |
| testis | UBERON:0000473 | 81.08 | gold quality |
| right testis | UBERON:0004534 | 79.80 | gold quality |
| adrenal tissue | UBERON:0018303 | 75.61 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 74.34 | gold quality |
| sural nerve | UBERON:0015488 | 61.42 | silver quality |
| stomach | UBERON:0000945 | 59.52 | gold quality |
| urinary bladder | UBERON:0001255 | 59.34 | silver quality |
| uterine cervix | UBERON:0000002 | 59.28 | gold quality |
| blood | UBERON:0000178 | 56.28 | gold quality |
| multicellular organism | UBERON:0000468 | 55.72 | gold quality |
| monocyte | CL:0000576 | 54.52 | gold quality |
| calcaneal tendon | UBERON:0003701 | 54.11 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 53.83 | gold quality |
| prefrontal cortex | UBERON:0000451 | 53.51 | gold quality |
| lung | UBERON:0002048 | 52.92 | gold quality |
| adrenal gland | UBERON:0002369 | 52.58 | gold quality |
| endometrium | UBERON:0001295 | 52.48 | silver quality |
| kidney | UBERON:0002113 | 52.46 | gold quality |
| primary visual cortex | UBERON:0002436 | 52.41 | gold quality |
| intestine | UBERON:0000160 | 51.98 | gold quality |
| cortex of kidney | UBERON:0001225 | 50.94 | silver quality |
| pancreas | UBERON:0001264 | 50.24 | silver quality |
| heart | UBERON:0000948 | 50.09 | gold quality |
| liver | UBERON:0002107 | 49.46 | silver quality |
| prostate gland | UBERON:0002367 | 49.15 | gold quality |
| tibial nerve | UBERON:0001323 | 49.04 | gold quality |
| gastrocnemius | UBERON:0001388 | 48.49 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 4.40 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 25)
- The results suggest that loc285194 is a p53-regulated tumor suppressor, which acts in part through repression of miR-211. (PMID:23558749)
- LOC285194 might be a novel prognostic indicator in colorectal cancer. (PMID:23680400)
- Decreased expression of LOC285194 could serve as a molecular marker to predict the clinical outcome of Esophageal squamous cell carcinoma patients after surgery, and select patients who would benefit from preoperative Chemoradiotherapy. (PMID:25169763)
- Low expression of TUSC7 is associated with osteosarcoma. (PMID:26781978)
- A three-lncRNA signature (LOC285194, RP11-462C24.1 and Nbla12061) identified via stepwise regression analysis showed potential as a diagnostic marker for colorectal cancer. (PMID:27683121)
- Ectopic expression of TUSC7 in HCT116 and SW480 cells significantly inhibited cell proliferation rate. There were 2 binding sites of miR-211-3p within the sequence of TUSC7 and TUSC7 expression level was negatively correlated with miR-211-3p. (PMID:28214867)
- long non-coding RNA TUSC7 was underexpressed in endometrial carcinoma, especially in endometrial carcinoma chemotherapy-resistant tissues and cell lines and acted as a potential tumor suppressor gene to inhibit cell growth as well as advance the chemotherapy sensitivity through targeted silencing of miR-23b, which might provide a new therapeutic target to endometrial carcinoma (PMID:28653877)
- TUSC7 was an independent prognostic indicator for overall survival and disease free survival. (PMID:28925483)
- Low expression of TUSC7 is associated with temozolomide resistance in glioblastoma. (PMID:29397407)
- These findings suggested TUSC7 suppressed chemotherapy resistance of ESCC by downregulating miR-224 to modulate DESC1/EGFR/AKT pathway. (PMID:29530057)
- Study results revealed that the expression of LOC285194 was significantly lower in non-small cell lung cancer (NSCLC) tumor tissues when compared with the corresponding non-tumor tissues. Its expression was correlated with the tumor size, disease-free survival, and overall survival rates. RNA protein interaction analysis revealed that p53 was the direct binding target of LOC285194 in NSCLC. (PMID:30542733)
- overexpression of TUSC7 inhibited Colorectal cancer (CRC) cell proliferation, metastasis, invasion and epithelialmesenchymal transition These findings indicated that TUSC7 is involved in CRC development. (PMID:31002365)
- This study demonstrated that decreased level of lncRNA loc285194 was associated with poor clinical outcomes for patients with different types of cancer, supporting a promising potential biomarker for prognosis and metastasis in human cancers.[systematic review and meta-analysis] (PMID:31054796)
- TUSC7 was downexpressed in EC tissues and cell lines, and TUSC7 upregulation could remarkably inhibit cell proliferation, cycle progression and metastasis in EC cells. (PMID:31200002)
- TUSC-7 was proved to be one strong suppressive lnc-RNA in lung adenocarcinoma stem cells, functioning through inactivating NOTCH signaling, and the turbulence on division modes precisely pointed to the key mechanisms of stem cells’ renewal. (PMID:31279783)
- Decreased expression of long non-coding LOC285194 predicts tumour progression and poor prognosis of hepatocellular carcinoma after curative hepatectomy. (PMID:31494574)
- Long non-coding RNA TUSC7 suppresses osteosarcoma by targeting miR-211. (PMID:31652435)
- Long non-coding RNA LOC285194 in cancer. (PMID:31837299)
- LncRNA LOC285194 modulates gastric carcinoma progression through activating Wnt/beta-catenin signaling pathway. (PMID:31991056)
- LOC285194 inhibits proliferation of human keratinocytes through regulating miR-616/GATA3 pathway. (PMID:32439362)
- Downregulation of long noncoding RNA TUSC7 promoted cell growth, invasion and migration through sponging with miR-616-5p/GSK3beta pathway in ovarian cancer. (PMID:32706063)
- [Serum level of lncRNA TUSC7 in patients with esophageal squamous cell carcinoma and its role in promoting tumor cell migration and invasion]. (PMID:32897196)
- Long non-coding RNA TUSC7 suppressed colorectal cancer progression via regulation of miR-23b/PDE7A Axis. (PMID:33370523)
- lncRNA TUSC7 inhibits osteosarcoma progression through the miR181a/RASSF6 axis. (PMID:33416181)
- A Proposed TUSC7/miR-211/Nurr1 ceRNET Might Potentially be Disturbed by a cer-SNP rs2615499 in Breast Cancer. (PMID:35296964)
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.