MIR558

gene
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Also known as hsa-mir-558

Summary

MIR558 (microRNA 558, HGNC:32814) is a microRNA gene on chromosome 2p22.3.

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 693143 — 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:32814
Approved symbolMIR558
NamemicroRNA 558
Location2p22.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-558
Ensembl geneENSG00000207653
Ensembl biotypemiRNA
OMIM616473
Entrez693143
RNAcentralURS00006DB970 — miRNA, 94 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000384920

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000384920 — 1 exons

ExonStartEnd
ENSE000014999273253215332532246

Expression profiles

Bgee: expression breadth broad, 77 present calls, max score 77.97.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830377.97gold quality
bloodUBERON:000017877.26gold quality
adult mammalian kidneyUBERON:000008275.05gold quality
muscle of legUBERON:000138373.85gold quality
kidneyUBERON:000211373.65gold quality
calcaneal tendonUBERON:000370173.63gold quality
monocyteCL:000057673.58gold quality
endometriumUBERON:000129573.56gold quality
gastrocnemiusUBERON:000138873.00gold quality
stomachUBERON:000094572.99gold quality
corpus callosumUBERON:000233672.82gold quality
amygdalaUBERON:000187671.27gold quality
adrenal glandUBERON:000236971.06gold quality
C1 segment of cervical spinal cordUBERON:000646970.98gold quality
liverUBERON:000210770.80gold quality
heartUBERON:000094870.72gold quality
left coronary arteryUBERON:000162669.65gold quality
body of pancreasUBERON:000115069.57gold quality
thoracic mammary glandUBERON:000520069.55gold quality
colonUBERON:000115568.64gold quality
lungUBERON:000204868.52gold quality
intestineUBERON:000016068.29gold quality
muscle layer of sigmoid colonUBERON:003580568.07gold quality
right atrium auricular regionUBERON:000663168.05gold quality
transverse colonUBERON:000115767.92gold quality
body of stomachUBERON:000116167.91gold quality
esophagogastric junction muscularis propriaUBERON:003584167.88gold quality
tibial arteryUBERON:000761067.76gold quality
heart left ventricleUBERON:000208467.68gold quality
popliteal arteryUBERON:000225067.63gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.31

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 11)

  • cartilage homeostasis is influenced by miR-558 which directly targets cyclooxygenase-2 and regulates IL-1beta-stimulated catabolic effects in human chondrocytes (PMID:23611898)
  • miRNA-558 promotes tumorigenesis and aggressiveness of neuroblastoma cells through activating the transcription of heparanase (PMID:25616966)
  • miR-558 facilitates the expression of HIF-2alpha through binding to its 5’-UTR, thus promoting the tumorigenesis and aggressiveness of neuroblastoma (PMID:27276678)
  • ATKK was validated as a target gene of miR-558, and upregulation of miR-558 was observed in radioresistant lung cancer cells. Additionally, ectopic overexpression of ATKK partially but significantly reduced the miR-558-induced radioresistance. (PMID:27485693)
  • miR-558 facilitates the progression of gastric cancer through directly targeting the HPSE promoter to attenuate Smad4-mediated repression of HPSE expression. (PMID:27685626)
  • Over-expression of circHIPK3 effectively inhibits migration, invasion, and angiogenesis of bladder cancer cells in vitro and suppresses bladder cancer growth and metastasis in vivo Mechanistic studies reveal that circHIPK3 contains two critical binding sites for the microRNA miR-558 and can abundantly sponge miR-558 to suppress the expression of heparanase (HPSE). (PMID:28794202)
  • Upregulated long noncoding RNA Linc00261 in pre-eclampsia and its effect on trophoblast invasion and migration via regulating miR-558/TIMP4 signaling pathway. (PMID:30891826)
  • A novel circular RNA, hsa_circ_0030998 suppresses lung cancer tumorigenesis and Taxol resistance by sponging miR-558. (PMID:33190405)
  • miR-558 Reduces the Damage of HBE Cells Exposed to Cigarette Smoke Extract by Targeting TNFRSF1A and Inactivating TAK1/MAPK/NF-kappaB Pathway. (PMID:33459100)
  • Circ-OPHN1 suppresses the proliferation, migration, and invasion of trophoblast cells through mediating miR-558/THBS2 axis. (PMID:35277867)
  • Re-expression of circ_0043610 contributes to trophoblast dysfunction through the miR-558/RYBP pathway in preeclampsia. (PMID:35908953)

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.