MIR762
gene geneOn this page
Also known as hsa-mir-762
Summary
MIR762 (microRNA 762, HGNC:37303) is a microRNA gene on chromosome 16p11.2.
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 100313837 — 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:37303 |
| Approved symbol | MIR762 |
| Name | microRNA 762 |
| Location | 16p11.2 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-762 |
| Ensembl gene | ENSG00000211591 |
| Ensembl biotype | miRNA |
| Entrez | 100313837 |
| RNAcentral | URS000075DA19 — miRNA, 83 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000390236
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000390236 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001507663 | 30893903 | 30893985 |
Expression profiles
Bgee: expression breadth tissue_specific, 2 present calls, max score 82.04.
Top tissues by expression
2 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| anterior cingulate cortex | UBERON:0009835 | 82.04 | gold quality |
| stomach | UBERON:0000945 | 76.78 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 10)
- a complex relationship between tear induction of miR-762, its modulation of innate defense genes, and P. aeruginosa internalization (PMID:23469087)
- Interferon regulatory factor 7 (IRF7) is a direct target of miR-762 and overexpression of miR-762 reduced expression of IRF7. (PMID:26597380)
- Aberrant levels of plasmic miR-144-3p and miR-762 were associated with Grave Disease, which may be biomarkers for Grave disease diagnosis. (PMID:30949910)
- MiR-762 promotes trophoblast cell epithelial-mesenchymal transition (EMT) by targeting directly Grhl2 gene 3’UTR. miR-762 was downregulated in placentas of patients with pre-eclampsia. (PMID:31354028)
- MicroRNA 762 (miR-762) expression is upregulated in gefitinib-resistant non-small-cell lung cancer (NSCLC) tissues and cells, and this upregulation predicts a poor post-chemotherapy prognosis in NSCLC patients. miR-762 upregulation, induced by IL-6 signaling, significantly enhances cell survival and renders NSCLC cells unresponsiveness to gefitinib-elicited cell death. (PMID:31823748)
- Circular RNA FAM114A2 suppresses progression of bladder cancer via regulating NP63 by sponging miR-762. (PMID:31969560)
- Identification of Circulating miR-762 as a Novel Diagnostic and Prognostic Biomarker for Non-Small Cell Lung Cancer. (PMID:33317398)
- Circ_0011460 upregulates HTRA1 expression by sponging miR-762 to suppress HTR8/SVneo cell growth, migration, and invasion. (PMID:34270834)
- A novel miRNA-762/NFIX pathway modulates LPS-induced acute lung injury. (PMID:34492536)
- Exosomes from human induced pluripotent stem cells-derived keratinocytes accelerate burn wound healing through miR-762 mediated promotion of keratinocytes and endothelial cells migration. (PMID:35729564)
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.