MIR3609

gene
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Also known as hsa-mir-3609

Summary

MIR3609 (microRNA 3609, HGNC:38956) is a microRNA gene on chromosome 7q22.1.

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 100500819 — 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:38956
Approved symbolMIR3609
NamemicroRNA 3609
Location7q22.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3609
Ensembl geneENSG00000266019
Ensembl biotypemiRNA
Entrez100500819
RNAcentralURS000075D1DB — ncRNA, 80 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000582661

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000582661 — 1 exons

ExonStartEnd
ENSE000026891839888165098881729

Expression profiles

Bgee: expression breadth broad, 70 present calls, max score 99.91.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370199.91gold quality
sural nerveUBERON:001548899.17gold quality
kidneyUBERON:000211383.78gold quality
bloodUBERON:000017880.06gold quality
adult mammalian kidneyUBERON:000008279.26gold quality
corpus callosumUBERON:000233677.72gold quality
placentaUBERON:000198777.38gold quality
C1 segment of cervical spinal cordUBERON:000646974.26gold quality
monocyteCL:000057674.14gold quality
liverUBERON:000210773.95gold quality
endometriumUBERON:000129572.69gold quality
islet of LangerhansUBERON:000000672.40gold quality
stomachUBERON:000094571.43gold quality
heartUBERON:000094870.68gold quality
lungUBERON:000204870.07gold quality
gastrocnemiusUBERON:000138870.06gold quality
right atrium auricular regionUBERON:000663169.56gold quality
tibial nerveUBERON:000132368.73gold quality
left adrenal glandUBERON:000123466.53gold quality
heart left ventricleUBERON:000208466.40gold quality
body of stomachUBERON:000116166.38gold quality
tibial arteryUBERON:000761065.97gold quality
body of pancreasUBERON:000115065.63gold quality
esophagus mucosaUBERON:000246965.61gold quality
esophagogastric junction muscularis propriaUBERON:003584165.61gold quality
left ovaryUBERON:000211965.51gold quality
esophagusUBERON:000104365.48gold quality
Ammon’s hornUBERON:000195465.07gold quality
intestineUBERON:000016064.97gold quality
lower esophagus muscularis layerUBERON:003583364.81gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.55

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • low miR-3609 expression and high PD-L1 expression were correlated with poor prognosis in breast cancer patients. Therefore, restoration of miR-3609 expression may sensitize breast cancer to adriamycin by blocking PD-L1 expression. (PMID:30904483)

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.