MIR1298
gene geneOn this page
Also known as hsa-mir-1298
Summary
MIR1298 (microRNA 1298, HGNC:35258) is a microRNA gene on chromosome Xq23.
microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop.
Source: NCBI Gene 100302153 — RefSeq curated summary.
At a glance
- Gene type: non-coding (miRNA) — 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:35258 |
| Approved symbol | MIR1298 |
| Name | microRNA 1298 |
| Location | Xq23 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-1298 |
| Ensembl gene | ENSG00000221710 |
| Ensembl biotype | miRNA |
| Entrez | 100302153 |
| RNAcentral | URS000075BA87 — miRNA, 112 nt, 4 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408783
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408783 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001565418 | 114715233 | 114715344 |
Expression profiles
Bgee: expression breadth broad, 22 present calls, max score 77.62.
Top tissues by expression
22 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 77.62 | gold quality |
| corpus callosum | UBERON:0002336 | 75.70 | gold quality |
| tibial artery | UBERON:0007610 | 71.76 | gold quality |
| right atrium auricular region | UBERON:0006631 | 70.80 | gold quality |
| transverse colon | UBERON:0001157 | 70.59 | gold quality |
| right lobe of liver | UBERON:0001114 | 70.08 | gold quality |
| ascending aorta | UBERON:0001496 | 69.71 | gold quality |
| esophagus mucosa | UBERON:0002469 | 69.66 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 69.62 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 66.49 | gold quality |
| prostate gland | UBERON:0002367 | 66.35 | gold quality |
| lung | UBERON:0002048 | 65.15 | gold quality |
| hypothalamus | UBERON:0001898 | 65.13 | gold quality |
| skin of abdomen | UBERON:0001416 | 65.03 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 64.81 | gold quality |
| tibial nerve | UBERON:0001323 | 64.53 | gold quality |
| vagina | UBERON:0000996 | 64.05 | gold quality |
| caudate nucleus | UBERON:0001873 | 63.41 | gold quality |
| nucleus accumbens | UBERON:0001882 | 62.98 | gold quality |
| putamen | UBERON:0001874 | 57.30 | gold quality |
| left testis | UBERON:0004533 | 47.26 | gold quality |
| right testis | UBERON:0004534 | 46.95 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.33 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 15)
- demonstrate a specific role of the upstream DNA methylation/miR-1298/Connexin 43 pathway in regulating VSMC function (PMID:26025955)
- Silencing of FAK or LAMB3 recapitulated the synthetic lethal effects of miR-1298 expression in KRAS-driven cancer cells, whereas coexpression of both proteins was critical to rescue miR-1298-induced cell death. (PMID:27698189)
- MicroRNA-1298-5p inhibits cell proliferation and the invasiveness of bladder cancer cells via down-regulation of connexin 43. (PMID:31600451)
- that the downregulation of miR-1298 predicts poor prognosis of non-small cell lung cancer (PMID:31801557)
- MicroRNA-1298-3p inhibits proliferation and invasion of glioma cells by downregulating Nidogen-1. (PMID:32355035)
- microRNA-1298 inhibits the malignant behaviors of breast cancer cells via targeting ADAM9. (PMID:33146718)
- Circular RNA circ_0003028 contributes to tumorigenesis by regulating GOT2 via miR-1298-5p in non-small cell lung cancer. (PMID:34077306)
- Inhibition of miR-1298-5p attenuates sepsis lung injury by targeting SOCS6. (PMID:34100174)
- Overexpression of miR-1298 attenuates myocardial ischemia-reperfusion injury by targeting PP2A. (PMID:34351558)
- LncRNA OSER1-AS1 regulates the inflammation and apoptosis of rheumatoid arthritis fibroblast like synoviocytes via regulating miR-1298-5p/E2F1 axis. (PMID:35164656)
- MiR-1298-5p level downregulation induced by Helicobacter pylori infection inhibits autophagy and promotes gastric cancer development by targeting MAP2K6. (PMID:35192930)
- Circular RNA hsa_circ_0119412 contributes to tumorigenesis of gastric cancer via the regulation of the miR-1298-5p/zinc finger BED-type containing 3 (ZBED3) axis. (PMID:35200111)
- The dual role of glioma exosomal microRNAs: glioma eliminates tumor suppressor miR-1298-5p via exosomes to promote immunosuppressive effects of MDSCs. (PMID:35501306)
- MicroRNA-1298-3p induces tumor-suppressive effects in human cervical cancer cells via post-transcriptional suppression of ONECUT2. (PMID:36508388)
- MicroRNA-1298-5p in granulosa cells facilitates cell autophagy in polycystic ovary syndrome by suppressing glutathione-disulfide reductase. (PMID:36781484)
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.