LINC00857
gene geneOn this page
Also known as HUMT
Summary
LINC00857 (long intergenic non-protein coding RNA 857, HGNC:45114) is a long non-coding RNA gene on chromosome 10q22.3.
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:45114 |
| Approved symbol | LINC00857 |
| Name | long intergenic non-protein coding RNA 857 |
| Location | 10q22.3 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | HUMT |
| Ensembl gene | ENSG00000237523 |
| Ensembl biotype | lncRNA |
| Entrez | 439990 |
| RNAcentral | URS000075AEB1 — lncRNA, 2171 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 14 — 14 lncRNA
ENST00000422847, ENST00000432308, ENST00000660450, ENST00000671081, ENST00000819791, ENST00000819792, ENST00000819793, ENST00000819794, ENST00000819795, ENST00000819796, ENST00000819797, ENST00000819798, ENST00000819799, ENST00000819800
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000422847 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001788315 | 80207710 | 80208231 |
| ENSE00004225066 | 80218019 | 80219657 |
Expression profiles
Bgee: expression breadth ubiquitous, 152 present calls, max score 79.32.
FANTOM5 (CAGE): breadth broad, TPM avg 1.2316 / max 30.4134, expressed in 653 samples.
FANTOM5 promoters (3 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 105848 | 0.7961 | 487 |
| 105847 | 0.3541 | 200 |
| 105849 | 0.0815 | 31 |
Top tissues by expression
238 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| bone marrow cell | CL:0002092 | 79.32 | gold quality |
| buccal mucosa cell | CL:0002336 | 76.84 | silver quality |
| colonic epithelium | UBERON:0000397 | 75.24 | gold quality |
| islet of Langerhans | UBERON:0000006 | 70.16 | gold quality |
| ascending aorta | UBERON:0001496 | 70.01 | gold quality |
| thoracic aorta | UBERON:0001515 | 69.93 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 68.62 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 68.17 | gold quality |
| duodenum | UBERON:0002114 | 68.04 | gold quality |
| stromal cell of endometrium | CL:0002255 | 67.98 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 67.41 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 67.07 | gold quality |
| right coronary artery | UBERON:0001625 | 66.90 | gold quality |
| lower esophagus | UBERON:0013473 | 66.54 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 66.53 | gold quality |
| gall bladder | UBERON:0002110 | 66.37 | gold quality |
| rectum | UBERON:0001052 | 65.98 | gold quality |
| aorta | UBERON:0000947 | 65.14 | gold quality |
| left uterine tube | UBERON:0001303 | 65.09 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 64.88 | gold quality |
| endocervix | UBERON:0000458 | 64.82 | gold quality |
| small intestine | UBERON:0002108 | 64.66 | gold quality |
| esophagus | UBERON:0001043 | 64.56 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 64.46 | gold quality |
| left ovary | UBERON:0002119 | 64.33 | gold quality |
| ectocervix | UBERON:0012249 | 64.32 | gold quality |
| left coronary artery | UBERON:0001626 | 63.84 | gold quality |
| transverse colon | UBERON:0001157 | 63.77 | gold quality |
| body of uterus | UBERON:0009853 | 63.54 | gold quality |
| jejunal mucosa | UBERON:0000399 | 63.37 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.09 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 12)
- Overexpression of LINC00857 increased cancer cell proliferation, colony formation and invasion. Mechanistic analyses indicated that LINC00857 mediates tumor progression via cell cycle regulation. (PMID:26862852)
- Long non-coding RNA HUMT hypomethylation promotes lymphangiogenesis and metastasis via activating FOXK1 transcription in triple-negative breast cancer. (PMID:32138762)
- LncRNA LINC00857 regulates the progression and glycolysis in ovarian cancer by modulating the Hippo signaling pathway. (PMID:32918541)
- LINC00857 contributes to proliferation and lymphomagenesis by regulating miR-370-3p/CBX3 axis in diffuse large B-cell lymphoma. (PMID:33657224)
- LncRNA LINC00857 strengthens the malignancy behaviors of pancreatic adenocarcinoma cells by serving as a competing endogenous RNA for miR-340-5p to upregulate TGFA expression. (PMID:33661995)
- LINC00857 promotes colorectal cancer progression by sponging miR-150-5p and upregulating HMGB3 (high mobility group box 3) expression. (PMID:34753396)
- Knockdown of long noncoding RNA HUMT inhibits the proliferation and metastasis by regulating miR-455-5p/LRP4 axis in hepatocellular carcinoma. (PMID:35293286)
- Oncogenic LINC00857 recruits TFAP2C to elevate FAT1 expression in gastric cancer. (PMID:35524544)
- Regulation of Transcription Factor YAP-TEAD by Non-coding RNA LINC00857 and the Inhibitory Effects on Ovarian Cancer Cell Proliferation. (PMID:35869712)
- Mutant p53 driven-LINC00857, a protein scaffold between FOXM1 and deubiquitinase OTUB1, promotes the metastasis of pancreatic cancer. (PMID:36272615)
- Functions, mechanisms, and clinical applications of lncRNA LINC00857 in cancer pathogenesis. (PMID:37378889)
- Abnormal methylation mediated upregulation of LINC00857 boosts malignant progression of lung adenocarcinoma by modulating the miR-486-5p/NEK2 axis. (PMID:38721812)
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.