MIR210HG
gene geneOn this page
Summary
MIR210HG (MIR210 host gene, HGNC:39524) is a long non-coding RNA gene on chromosome 11p15.5.
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:39524 |
| Approved symbol | MIR210HG |
| Name | MIR210 host gene |
| Location | 11p15.5 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000247095 |
| Ensembl biotype | lncRNA |
| Entrez | 100506211 |
| RNAcentral | URS000075D777 — lncRNA, 2303 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 15 — 15 lncRNA
ENST00000500447, ENST00000528245, ENST00000533920, ENST00000534540, ENST00000665964, ENST00000688743, ENST00000688898, ENST00000692695, ENST00000702592, ENST00000827434, ENST00000827435, ENST00000827436, ENST00000827437, ENST00000827438, ENST00000827439
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000500447 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00004239319 | 568352 | 568449 |
| ENSE00004239325 | 565660 | 567555 |
Expression profiles
Bgee: expression breadth ubiquitous, 134 present calls, max score 97.60.
FANTOM5 (CAGE): breadth broad, TPM avg 1.1927 / max 31.8978, expressed in 605 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 117779 | 1.1927 | 605 |
Top tissues by expression
134 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| lower esophagus mucosa | UBERON:0035834 | 97.60 | gold quality |
| esophagus mucosa | UBERON:0002469 | 94.27 | gold quality |
| skin of leg | UBERON:0001511 | 94.09 | gold quality |
| zone of skin | UBERON:0000014 | 93.84 | gold quality |
| skin of abdomen | UBERON:0001416 | 93.74 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 90.42 | gold quality |
| vagina | UBERON:0000996 | 90.25 | gold quality |
| right uterine tube | UBERON:0001302 | 89.97 | gold quality |
| esophagus | UBERON:0001043 | 89.57 | gold quality |
| apex of heart | UBERON:0002098 | 89.40 | gold quality |
| metanephros cortex | UBERON:0010533 | 89.06 | gold quality |
| right atrium auricular region | UBERON:0006631 | 86.56 | gold quality |
| minor salivary gland | UBERON:0001830 | 85.56 | gold quality |
| transverse colon | UBERON:0001157 | 85.23 | gold quality |
| saliva-secreting gland | UBERON:0001044 | 84.93 | gold quality |
| lower esophagus | UBERON:0013473 | 84.79 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 84.73 | gold quality |
| right lobe of liver | UBERON:0001114 | 84.61 | gold quality |
| colonic epithelium | UBERON:0000397 | 84.44 | gold quality |
| heart left ventricle | UBERON:0002084 | 84.26 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 84.04 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 83.75 | gold quality |
| rectum | UBERON:0001052 | 83.44 | gold quality |
| cortex of kidney | UBERON:0001225 | 83.40 | gold quality |
| heart | UBERON:0000948 | 83.16 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 82.69 | gold quality |
| body of stomach | UBERON:0001161 | 82.51 | gold quality |
| tibial artery | UBERON:0007610 | 82.29 | gold quality |
| popliteal artery | UBERON:0002250 | 82.27 | gold quality |
| small intestine | UBERON:0002108 | 82.07 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.78 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 14)
- The long noncoding RNA MIR210HG promotes tumor metastasis by acting as a ceRNA of miR-1226-3p to regulate mucin-1c expression in invasive breast cancer. (PMID:31399552)
- MIR210HG promotes cell proliferation and invasion by regulating miR-503-5p/TRAF4 axis in cervical cancer. (PMID:32087604)
- Long noncoding RNA expression profiling identifies MIR210HG as a novel molecule in severe preeclampsia. (PMID:33516697)
- MIR210HG regulates glycolysis, cell proliferation, and metastasis of pancreatic cancer cells through miR-125b-5p/HK2/PKM2 axis. (PMID:34110962)
- [Expression of lncRNA MIR210HG in preeclampsia placental tissue and its functional analysis]. (PMID:34154318)
- Hypoxia-inducible lncRNA MIR210HG interacting with OCT1 is involved in glioblastoma multiforme malignancy. (PMID:34897892)
- MIR210HG is aberrantly expressed in the seminal plasma of varicocele patients and associated with varicocele-related dyszoospermia. (PMID:35146790)
- The crucial role of LncRNA MIR210HG involved in the regulation of human cancer and other disease. (PMID:36088513)
- ceRNA network of lncRNA MIR210HG/miR-377-3p/LMX1A in malignant proliferation of glioma cells. (PMID:36197580)
- Hypoxia-inducible lncRNA MIR210HG promotes HIF1alpha expression by inhibiting miR-93-5p in renal tubular cells. (PMID:37029581)
- LncRNA MIR210HG promotes the proliferation, migration, and invasion of lung cancer cells by inhibiting the transcription of SH3GL3. (PMID:37916731)
- Pan-cancer analyses identify MIR210HG overexpression, epigenetic regulation and oncogenic role in human tumors and its interaction with the tumor microenvironment. (PMID:38242493)
- Transcriptomic Analyses and Experimental Validation Identified Immune-Related lncRNA-mRNA Pair MIR210HG-BPIFC Regulating the Progression of Hypertrophic Cardiomyopathy. (PMID:38474063)
- LncRNA MIR210HG promotes phenotype switching of pulmonary arterial smooth muscle cells through autophagy-dependent ferroptosis pathway. (PMID:38635022)
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.