MIR4655

gene
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Also known as hsa-mir-4655

Summary

MIR4655 (microRNA 4655, HGNC:41754) is a microRNA gene on chromosome 7p22.3.

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 100616160 — 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:41754
Approved symbolMIR4655
NamemicroRNA 4655
Location7p22.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4655
Ensembl geneENSG00000265089
Ensembl biotypemiRNA
Entrez100616160
RNAcentralURS000075EACC — ncRNA, 74 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000580817

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000580817 — 1 exons

ExonStartEnd
ENSE0000272375718441801844253

Expression profiles

Bgee: expression breadth broad, 59 present calls, max score 78.40.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017878.40gold quality
right lobe of liverUBERON:000111478.21gold quality
adrenal tissueUBERON:001830375.93gold quality
tibial arteryUBERON:000761075.16gold quality
liverUBERON:000210773.40gold quality
body of stomachUBERON:000116172.94gold quality
gastrocnemiusUBERON:000138872.61gold quality
monocyteCL:000057672.40gold quality
adult mammalian kidneyUBERON:000008271.86gold quality
stomachUBERON:000094570.10gold quality
right atrium auricular regionUBERON:000663169.08gold quality
left uterine tubeUBERON:000130368.75gold quality
lower esophagus muscularis layerUBERON:003583368.30gold quality
heart left ventricleUBERON:000208468.03gold quality
skin of abdomenUBERON:000141666.72gold quality
nucleus accumbensUBERON:000188265.99gold quality
Ammon’s hornUBERON:000195465.62gold quality
muscle layer of sigmoid colonUBERON:003580565.59gold quality
myometriumUBERON:000129665.55gold quality
ascending aortaUBERON:000149665.52gold quality
hypothalamusUBERON:000189865.38gold quality
esophagogastric junction muscularis propriaUBERON:003584165.34gold quality
body of pancreasUBERON:000115065.29gold quality
right frontal lobeUBERON:000281065.16gold quality
amygdalaUBERON:000187665.12gold quality
putamenUBERON:000187464.99gold quality
minor salivary glandUBERON:000183064.72gold quality
zone of skinUBERON:000001464.70gold quality
subcutaneous adipose tissueUBERON:000219064.40gold quality
left coronary arteryUBERON:000162664.37gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.20

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • Exosome-mediated miR-4655-3p contributes to UV radiation-induced bystander effects. (PMID:35688281)
  • Irradiated lung cancer cell-derived exosomes modulate macrophage polarization by inhibiting MID1 via miR-4655-5p. (PMID:36709645)

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.