MIR3189

gene
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Also known as hsa-mir-3189

Summary

MIR3189 (microRNA 3189, HGNC:38307) is a microRNA gene on chromosome 19p13.11.

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 100422943 — 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:38307
Approved symbolMIR3189
NamemicroRNA 3189
Location19p13.11
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3189
Ensembl geneENSG00000264175
Ensembl biotypemiRNA
Entrez100422943
RNAcentralURS000075DBDF — miRNA, 73 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000578735

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000578735 — 1 exons

ExonStartEnd
ENSE000027328591838656218386634

Expression profiles

Bgee: expression breadth broad, 100 present calls, max score 94.81.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
metanephros cortexUBERON:001053394.81gold quality
rectumUBERON:000105292.10gold quality
kidneyUBERON:000211391.75gold quality
duodenumUBERON:000211491.66gold quality
adult mammalian kidneyUBERON:000008290.59gold quality
placentaUBERON:000198788.31gold quality
urinary bladderUBERON:000125586.78gold quality
stomachUBERON:000094586.35gold quality
body of stomachUBERON:000116185.79gold quality
smooth muscle tissueUBERON:000113585.14gold quality
body of pancreasUBERON:000115084.72gold quality
prostate glandUBERON:000236783.75gold quality
pancreasUBERON:000126483.03gold quality
gall bladderUBERON:000211082.15gold quality
fundus of stomachUBERON:000116081.81gold quality
adrenal tissueUBERON:001830380.15gold quality
calcaneal tendonUBERON:000370179.45gold quality
liverUBERON:000210779.13gold quality
right lobe of liverUBERON:000111478.69gold quality
olfactory segment of nasal mucosaUBERON:000538678.64gold quality
islet of LangerhansUBERON:000000678.15gold quality
bloodUBERON:000017877.54gold quality
transverse colonUBERON:000115776.92gold quality
endometriumUBERON:000129576.55gold quality
endocervixUBERON:000045876.21gold quality
lungUBERON:000204876.19gold quality
gastrocnemiusUBERON:000138876.02gold quality
adenohypophysisUBERON:000219675.88gold quality
colonUBERON:000115575.59gold quality
intestineUBERON:000016074.90gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.26

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 5)

  • miR-3189-3p-mediated inhibition of tumor growth in vivo further supports the function of this microRNA as a tumor suppressor. (PMID:25645911)
  • miR-3189 is embedded in the intron of GDF15 gene. miR-3189 is a novel, primate-specific miRNA whose effects are mediated by both p53-dependent and p53-independent mechanisms. (PMID:25698447)
  • miR-3189-3p mimics enhanced the effects of the S100A4 siRNA on the inhibition of gastric cancer cell proliferation and migration by targeting CFL2. (PMID:29342841)
  • miR-3189-targeted GLUT3 repression by HDAC2 knockdown inhibits glioblastoma tumorigenesis through regulating glucose metabolism and proliferation. (PMID:35260183)
  • A novel interplay between PRC2 and miR-3189 regulates epithelial-mesenchymal transition (EMT) via modulating COL6A2 in glioblastoma. (PMID:38860406)

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.