MIR769

gene
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Also known as hsa-mir-769

Summary

MIR769 (microRNA 769, HGNC:33138) is a microRNA gene on chromosome 19q13.32.

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 768217 — 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:33138
Approved symbolMIR769
NamemicroRNA 769
Location19q13.32
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-769
Ensembl geneENSG00000211580
Ensembl biotypemiRNA
Entrez768217
RNAcentralURS000075D819 — miRNA, 118 nt, 5 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000390225

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000390225 — 1 exons

ExonStartEnd
ENSE000015076524601893246019049

Expression profiles

Bgee: expression breadth broad, 76 present calls, max score 78.53.

Top tissues by expression

76 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
monocyteCL:000057678.53gold quality
bloodUBERON:000017878.15gold quality
muscle of legUBERON:000138377.24gold quality
gastrocnemiusUBERON:000138874.39gold quality
adenohypophysisUBERON:000219674.14gold quality
bone marrowUBERON:000237172.59gold quality
heart left ventricleUBERON:000208470.92gold quality
left coronary arteryUBERON:000162670.73gold quality
adult mammalian kidneyUBERON:000008270.63gold quality
smooth muscle tissueUBERON:000113569.63gold quality
urinary bladderUBERON:000125569.54gold quality
right atrium auricular regionUBERON:000663169.33gold quality
body of uterusUBERON:000985369.25gold quality
tibial arteryUBERON:000761069.22gold quality
body of stomachUBERON:000116169.10gold quality
islet of LangerhansUBERON:000000669.06gold quality
stomachUBERON:000094568.56gold quality
lower esophagus muscularis layerUBERON:003583368.49gold quality
esophagogastric junction muscularis propriaUBERON:003584168.49gold quality
right adrenal gland cortexUBERON:003582768.20gold quality
right hemisphere of cerebellumUBERON:001489068.16gold quality
Brodmann (1909) area 9UBERON:001354067.76gold quality
body of pancreasUBERON:000115067.69gold quality
fundus of stomachUBERON:000116067.67gold quality
cerebellar hemisphereUBERON:000224567.61gold quality
placentaUBERON:000198767.50gold quality
esophagusUBERON:000104367.35gold quality
minor salivary glandUBERON:000183067.20gold quality
ascending aortaUBERON:000149667.02gold quality
lungUBERON:000204867.01gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.16

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 17)

  • miR-769-3p can functionally regulate NDRG1 during changes in oxygen concentration. (PMID:25081069)
  • miR-769 might act as a tumor promoter by targeting GSK3B during development of human melanoma. (PMID:27470346)
  • identified miR-769-5p, miR-320a and miR-22-3p as potential blood-based biomarkers for TB. In addition, miR-320a may represent a biomarker for drug-resistant TB. (PMID:28910318)
  • Epidermal growth factor receptor (EGFR) is identified as a direct target gene of miR-769-5p. (PMID:30601026)
  • the up-regulated expression of miR-769-5p contributed to Hepatocellular carcinoma progression possibly by targeting RYBP. (PMID:31545279)
  • MiR-769-5p inhibits cancer progression in oral squamous cell carcinoma by directly targeting JAK1/STAT3 pathway. (PMID:32064884)
  • A Novel Three-miRNA Signature Identified Using Bioinformatics Predicts Survival in Esophageal Carcinoma. (PMID:32104700)
  • MiR-769-5p functions as an oncogene by down-regulating RYBP expression in gastric cancer. (PMID:32633360)
  • Long non-coding RNA RP11-284F21.9 functions as a ceRNA regulating PPWD1 by competitively binding to miR-769-3p in cervical carcinoma. (PMID:32936290)
  • Long non-coding RNA HAND2-AS1 inhibits gastric cancer progression by suppressing TCEAL7 expression via targeting miR-769-5p. (PMID:32952069)
  • LncRNA H19 promotes keloid formation through targeting the miR-769-5p/EIF3A pathway. (PMID:33389493)
  • The novel circular RNA circ-PGAP3 retards cervical cancer growth by regulating the miR-769-5p/p53 axis. (PMID:33591461)
  • Knockdown of MALAT1 Inhibits the Progression of Chronic Periodontitis via Targeting miR-769-5p/HIF3A Axis. (PMID:33604388)
  • Involvement of miR-769-5p/Retinoic Acid Receptor Responder 1 Axis in the Progression of Osteosarcoma: Characterization of Potential Therapeutic Targets. (PMID:35152215)
  • Exosome-transmitted miR-769-5p confers cisplatin resistance and progression in gastric cancer by targeting CASP9 and promoting the ubiquitination degradation of p53. (PMID:35522909)
  • Circ_0084188 Regulates the progression of colorectal cancer through the miR-769-5p/KIF20A axis. (PMID:36763221)
  • CircRNA LOC729852 promotes bladder cancer progression by regulating macrophage polarization and recruitment via the miR-769-5p/IL-10 axis. (PMID:38506082)

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.

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