MIR548AM

gene
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Also known as hsa-mir-548am

Summary

MIR548AM (microRNA 548am, HGNC:41637) is a microRNA gene on chromosome Xp22.2.

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 100616428 — 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:41637
Approved symbolMIR548AM
NamemicroRNA 548am
LocationXp22.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-548am
Ensembl geneENSG00000265144
Ensembl biotypemiRNA
Entrez100616428
RNAcentralURS000075EC75 — miRNA, 74 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000584298

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000584298 — 1 exons

ExonStartEnd
ENSE000027006901662701216627085

Expression profiles

Bgee: expression breadth broad, 66 present calls, max score 76.22.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
endometriumUBERON:000129576.22gold quality
islet of LangerhansUBERON:000000674.72gold quality
muscle of legUBERON:000138374.27gold quality
stomachUBERON:000094573.00gold quality
bloodUBERON:000017872.07gold quality
monocyteCL:000057671.04gold quality
gastrocnemiusUBERON:000138870.34gold quality
right adrenal glandUBERON:000123369.29gold quality
heartUBERON:000094869.05gold quality
thoracic mammary glandUBERON:000520069.00gold quality
heart left ventricleUBERON:000208468.79gold quality
right lobe of liverUBERON:000111468.44gold quality
fundus of stomachUBERON:000116068.19gold quality
body of stomachUBERON:000116168.18gold quality
liverUBERON:000210767.91gold quality
right atrium auricular regionUBERON:000663167.71gold quality
lungUBERON:000204867.30gold quality
tibial arteryUBERON:000761067.12gold quality
body of pancreasUBERON:000115066.71gold quality
esophagogastric junction muscularis propriaUBERON:003584166.45gold quality
ascending aortaUBERON:000149666.36gold quality
left coronary arteryUBERON:000162666.06gold quality
lower esophagus muscularis layerUBERON:003583365.86gold quality
amygdalaUBERON:000187665.69gold quality
skin of legUBERON:000151165.68gold quality
body of uterusUBERON:000985365.42gold quality
adult mammalian kidneyUBERON:000008265.06gold quality
transverse colonUBERON:000115764.76gold quality
right hemisphere of cerebellumUBERON:001489064.69gold quality
subcutaneous adipose tissueUBERON:000219064.63gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.33

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • miR548am-5p can account for sex-dependent differences observed in the susceptibility to mitochondrial apoptosis of human dermal fibroblasts. (PMID:31511496)

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.