MIR369

gene
On 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

FieldValue
HGNC IDHGNC:31783
Approved symbolMIR369
NamemicroRNA 369
Location14q32.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-369
Ensembl geneENSG00000199025
Ensembl biotypemiRNA
OMIM611794
Entrez442914
RNAcentralURS000075D5A7 — 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

ExonStartEnd
ENSE00001436918101065598101065667

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):

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830394.72gold quality
skeletal muscle tissueUBERON:000113489.01gold quality
placentaUBERON:000198781.88gold quality
heart left ventricleUBERON:000208481.57gold quality
left ovaryUBERON:000211977.58gold quality
adrenal glandUBERON:000236976.57gold quality
liverUBERON:000210775.54gold quality
right adrenal glandUBERON:000123375.52gold quality
ovaryUBERON:000099275.44gold quality
muscle of legUBERON:000138374.82gold quality
right adrenal gland cortexUBERON:003582774.45gold quality
stomachUBERON:000094574.29gold quality
left adrenal glandUBERON:000123473.98gold quality
heartUBERON:000094873.32gold quality
left adrenal gland cortexUBERON:003582573.23gold quality
body of pancreasUBERON:000115072.67gold quality
monocyteCL:000057672.42gold quality
endometriumUBERON:000129571.86gold quality
body of stomachUBERON:000116171.69gold quality
gastrocnemiusUBERON:000138871.58gold quality
adipose tissueUBERON:000101371.56gold quality
vaginaUBERON:000099671.41gold quality
omental fat padUBERON:001041471.35gold quality
prefrontal cortexUBERON:000045171.32gold quality
lungUBERON:000204871.09gold quality
islet of LangerhansUBERON:000000671.06gold quality
bloodUBERON:000017869.93gold quality
saliva-secreting glandUBERON:000104469.74gold quality
intestineUBERON:000016068.53gold quality
body of uterusUBERON:000985368.35gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.