MIR548V

gene
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Also known as hsa-mir-548v

Summary

MIR548V (microRNA 548v, HGNC:38302) is a microRNA gene on chromosome 8p22.

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 100422850 — 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:38302
Approved symbolMIR548V
NamemicroRNA 548v
Location8p22
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-548v
Ensembl geneENSG00000265520
Ensembl biotypemiRNA
Entrez100422850
RNAcentralURS000075B80E — miRNA, 80 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000584165

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000584165 — 1 exons

ExonStartEnd
ENSE000027106471768157817681657

Expression profiles

Bgee: expression breadth ubiquitous, 103 present calls, max score 96.54.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
corpus callosumUBERON:000233696.54gold quality
sural nerveUBERON:001548894.23gold quality
calcaneal tendonUBERON:000370190.96gold quality
adrenal tissueUBERON:001830390.53gold quality
vermiform appendixUBERON:000115482.47gold quality
duodenumUBERON:000211482.27gold quality
bloodUBERON:000017880.95gold quality
liverUBERON:000210779.84gold quality
adult mammalian kidneyUBERON:000008277.32gold quality
endometriumUBERON:000129577.17gold quality
kidneyUBERON:000211377.04gold quality
muscle of legUBERON:000138376.61gold quality
placentaUBERON:000198776.51gold quality
fundus of stomachUBERON:000116074.96gold quality
gastrocnemiusUBERON:000138874.83gold quality
lower esophagus mucosaUBERON:003583474.48gold quality
stomachUBERON:000094574.39gold quality
rectumUBERON:000105273.95gold quality
prefrontal cortexUBERON:000045173.78gold quality
monocyteCL:000057673.09gold quality
olfactory segment of nasal mucosaUBERON:000538672.98gold quality
pancreasUBERON:000126472.91gold quality
body of pancreasUBERON:000115072.64gold quality
islet of LangerhansUBERON:000000672.42gold quality
right lobe of liverUBERON:000111472.07gold quality
adrenal glandUBERON:000236971.48gold quality
lymph nodeUBERON:000002971.46gold quality
heartUBERON:000094871.40gold quality
heart left ventricleUBERON:000208470.73gold quality
body of stomachUBERON:000116170.48gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.55

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • hsa-miR-548v controls the viscoelastic properties of human cardiomyocytes and improves their relaxation rates. (PMID:38165745)

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.