MIR548J

gene
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Also known as hsa-mir-548j

Summary

MIR548J (microRNA 548j, HGNC:35276) is a microRNA gene on chromosome 22q12.1.

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 100313914 — 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:35276
Approved symbolMIR548J
NamemicroRNA 548j
Location22q12.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-548j
Ensembl geneENSG00000221760
Ensembl biotypemiRNA
Entrez100313914
RNAcentralURS000075C407 — miRNA, 112 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000408833

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000408833 — 1 exons

ExonStartEnd
ENSE000015654682655521226555323

Expression profiles

Bgee: expression breadth broad, 70 present calls, max score 79.66.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
amygdalaUBERON:000187679.66gold quality
myometriumUBERON:000129679.17gold quality
bloodUBERON:000017878.02gold quality
monocyteCL:000057677.14gold quality
adult mammalian kidneyUBERON:000008275.67gold quality
body of pancreasUBERON:000115074.69gold quality
muscle of legUBERON:000138374.69gold quality
gastrocnemiusUBERON:000138874.55gold quality
kidneyUBERON:000211374.10gold quality
liverUBERON:000210773.69gold quality
lymph nodeUBERON:000002972.63gold quality
ascending aortaUBERON:000149671.20gold quality
esophagogastric junction muscularis propriaUBERON:003584170.24gold quality
thoracic aortaUBERON:000151570.19gold quality
body of stomachUBERON:000116170.17gold quality
tibial arteryUBERON:000761070.07gold quality
endometriumUBERON:000129569.67gold quality
stomachUBERON:000094569.15gold quality
lower esophagus muscularis layerUBERON:003583368.85gold quality
adrenal tissueUBERON:001830368.77gold quality
heart left ventricleUBERON:000208468.53gold quality
heartUBERON:000094868.48gold quality
omental fat padUBERON:001041468.46gold quality
vaginaUBERON:000099668.27gold quality
subcutaneous adipose tissueUBERON:000219067.67gold quality
colonUBERON:000115567.65gold quality
intestineUBERON:000016067.48gold quality
body of uterusUBERON:000985367.39gold quality
left adrenal glandUBERON:000123467.31gold quality
right hemisphere of cerebellumUBERON:001489066.58gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.32

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • MiR-548j, miR-548m, and miR-548d-5p have homologous binding sites in the mRNA of PTPN12 orthologous genes which encode PRTRSC, TEATDI, and STASAT oligopeptides, respectively (PMID:23957009)
  • miR-548j-5p regulates angiogenesis in peripheral artery disease. (PMID:35039547)

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.