MIR369
gene geneOn this page
Also known as hsa-mir-369
Summary
MIR369 (microRNA 369, HGNC:31783) is a microRNA gene on chromosome 14q32.31.
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 442914 — 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:31783 |
| Approved symbol | MIR369 |
| Name | microRNA 369 |
| Location | 14q32.31 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-369 |
| Ensembl gene | ENSG00000199025 |
| Ensembl biotype | miRNA |
| OMIM | 611794 |
| Entrez | 442914 |
| RNAcentral | URS000075D5A7 — miRNA, 70 nt, 19 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000362155
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000362155 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001436918 | 101065598 | 101065667 |
Expression profiles
Bgee: expression breadth broad, 74 present calls, max score 94.72.
Top tissues by expression
74 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adrenal tissue | UBERON:0018303 | 94.72 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 89.01 | gold quality |
| placenta | UBERON:0001987 | 81.88 | gold quality |
| heart left ventricle | UBERON:0002084 | 81.57 | gold quality |
| left ovary | UBERON:0002119 | 77.58 | gold quality |
| adrenal gland | UBERON:0002369 | 76.57 | gold quality |
| liver | UBERON:0002107 | 75.54 | gold quality |
| right adrenal gland | UBERON:0001233 | 75.52 | gold quality |
| ovary | UBERON:0000992 | 75.44 | gold quality |
| muscle of leg | UBERON:0001383 | 74.82 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 74.45 | gold quality |
| stomach | UBERON:0000945 | 74.29 | gold quality |
| left adrenal gland | UBERON:0001234 | 73.98 | gold quality |
| heart | UBERON:0000948 | 73.32 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 73.23 | gold quality |
| body of pancreas | UBERON:0001150 | 72.67 | gold quality |
| monocyte | CL:0000576 | 72.42 | gold quality |
| endometrium | UBERON:0001295 | 71.86 | gold quality |
| body of stomach | UBERON:0001161 | 71.69 | gold quality |
| gastrocnemius | UBERON:0001388 | 71.58 | gold quality |
| adipose tissue | UBERON:0001013 | 71.56 | gold quality |
| vagina | UBERON:0000996 | 71.41 | gold quality |
| omental fat pad | UBERON:0010414 | 71.35 | gold quality |
| prefrontal cortex | UBERON:0000451 | 71.32 | gold quality |
| lung | UBERON:0002048 | 71.09 | gold quality |
| islet of Langerhans | UBERON:0000006 | 71.06 | gold quality |
| blood | UBERON:0000178 | 69.93 | gold quality |
| saliva-secreting gland | UBERON:0001044 | 69.74 | gold quality |
| intestine | UBERON:0000160 | 68.53 | gold quality |
| body of uterus | UBERON:0009853 | 68.35 | 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 19)
- miR-369-5p and miR-371 as antagonistic up-stream regulators of adipogenic differentiation and this might be indirectly mediated by epigenetic modifications. (PMID:21660946)
- The presence of at least one C allele is associated with a decreased expression of OLR1 mRNA in the absence of hsa-miR369-3p de-regulation (PMID:21709374)
- Low miR-369 expression is associated with chronic rejection in Bronchiolitis Obliterans Syndrome patients following lung transplantation. (PMID:25649290)
- A unique role of the embryonic miR-369-HNRNPA2B1 axis in controlling metabolic enzyme function. (PMID:26176628)
- This study demonstrated that overexpression of miR-369-3p in glioblastoma cells inhibited their proliferation and migration in vitro. Mice implanted with glioblastoma cells overexpressing miR369-3p. (PMID:27573219)
- aberrant expression of miR-369-3p might play a crucial role in the development HSCR by regulating SOX4 expression, which may infer that it is an effective diagnostic target in the pathogenesis of HSCR, but investigation is still needed to explore the underlying mechanism. (PMID:28412032)
- LncRNA OIP5-AS1 suppressed cell viability, promoted radio-induced apoptosis, and enhanced the radiosensitivity of CRC cells by regulating DYRK1A expression through miR-369-3p. (PMID:29773344)
- downregulation of miR-369-3p and consequent upregulation of its target TSPAN13 appear to be involved in pathophysiology of papillary thyroid cancer (PMID:30114378)
- These findings provide convincing evidence that both the 5p and 3p arms of miRNA co-expressed in gastric cancer (GC) and DNA methylation-induced miR-369 signaling contribute to GC progression. (PMID:31162777)
- LncRNA SOX2 overlapping transcript (SOX2-OT) expression was conspicuously elevated in prostate cancer (PC) tissues and cells. Silenced SOX2-OT could repress PC cell proliferation and migration. SOX2-OT bound with miR-369-3p and negatively correlated with miR-369-3p in PC. Cofilin 2 (CFL2) was found to be a downstream target gene of miR-369-3p. (PMID:31623830)
- Fibroblastderived exosomal microRNA369 potentiates migration and invasion of lung squamous cell carcinoma cells via NF1mediated MAPK signaling pathway. (PMID:32467987)
- MiR-369-3p inhibits tumorigenesis of hepatocellular carcinoma by binding to PAX6. (PMID:32608213)
- Knockdown of long noncoding RNA DLEU2 suppresses idiopathic pulmonary fibrosis by regulating the microRNA3693p/TRIM2 axis. (PMID:33760118)
- miR-369-3p serves as prognostic factor and regulates cancer progression of hepatocellular carcinoma. (PMID:33792408)
- [Molecular mechanism of miR-369-3p regulating hepatocellular carcinoma cell proliferation and apoptosis by targeting ACTN4]. (PMID:34794217)
- MiR-369-5p inhibits the proliferation and migration of hepatocellular carcinoma cells by down-regulating HOXA13 expression. (PMID:34979376)
- A Novel Mechanism of Immunoproteasome Regulation via miR-369-3p in Intestinal Inflammatory Response. (PMID:36430249)
- miR-369-3p Modulates Intestinal Inflammatory Response via BRCC3/NLRP3 Inflammasome Axis. (PMID:37681916)
- Anti-Inflammatory Effects of miR-369-3p via PDE4B in Intestinal Inflammatory Response. (PMID:39126032)
Cross-species orthologs
0 orthologs
Paralogs (16): MIR494 (ENSG00000194717), MIR377 (ENSG00000199015), MIR381 (ENSG00000199020), MIR323A (ENSG00000199069), MIR410 (ENSG00000199092), MIR409 (ENSG00000199107), MIR539 (ENSG00000202560), MIR487A (ENSG00000207742), MIR487B (ENSG00000207754), MIR656 (ENSG00000207959), MIR496 (ENSG00000207961), MIR154 (ENSG00000207978), MIR323B (ENSG00000208004), MIR1185-1 (ENSG00000221525), MIR1185-2 (ENSG00000221614), MIR382 (ENSG00000283170)
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.