MIR4730

gene
On this page

Also known as hsa-mir-4730

Summary

MIR4730 (microRNA 4730, HGNC:41880) is a microRNA gene on chromosome 17q25.3.

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 100616359 — 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:41880
Approved symbolMIR4730
NamemicroRNA 4730
Location17q25.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4730
Ensembl geneENSG00000264961
Ensembl biotypemiRNA
Entrez100616359
RNAcentralURS000075CB67 — ncRNA, 76 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000584535

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000584535 — 1 exons

ExonStartEnd
ENSE000027272358041941880419493

Expression profiles

Bgee: expression breadth ubiquitous, 108 present calls, max score 85.97.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830385.97gold quality
duodenumUBERON:000211483.74gold quality
vermiform appendixUBERON:000115482.09gold quality
bone marrowUBERON:000237181.51gold quality
placentaUBERON:000198780.21gold quality
prefrontal cortexUBERON:000045179.00gold quality
right hemisphere of cerebellumUBERON:001489078.40gold quality
cerebellar hemisphereUBERON:000224577.54gold quality
endometriumUBERON:000129575.55gold quality
muscle of legUBERON:000138375.30gold quality
lymph nodeUBERON:000002975.22gold quality
bloodUBERON:000017874.96gold quality
gastrocnemiusUBERON:000138874.68gold quality
adult mammalian kidneyUBERON:000008274.49gold quality
monocyteCL:000057674.32gold quality
apex of heartUBERON:000209874.31gold quality
kidneyUBERON:000211373.38gold quality
heart left ventricleUBERON:000208473.19gold quality
smooth muscle tissueUBERON:000113572.77gold quality
stomachUBERON:000094572.44gold quality
granulocyteCL:000009472.39gold quality
body of pancreasUBERON:000115072.35gold quality
right ovaryUBERON:000211872.24gold quality
rectumUBERON:000105272.20gold quality
gall bladderUBERON:000211072.12gold quality
fundus of stomachUBERON:000116071.96gold quality
body of stomachUBERON:000116171.89gold quality
heartUBERON:000094871.80gold quality
right coronary arteryUBERON:000162571.78gold quality
myometriumUBERON:000129671.61gold 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)

  • Hsa-miR-4730 as a new and potential diagnostic and prognostic indicators for pancreatic cancer. (PMID:32964968)
  • miR4730 suppresses the progression of liver cancer by targeting the high mobility group A1 pathway. (PMID:35485281)

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.