MIR618

gene
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Also known as hsa-mir-618

Summary

MIR618 (microRNA 618, HGNC:32874) is a microRNA gene on chromosome 12q21.31.

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 693203 — 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:32874
Approved symbolMIR618
NamemicroRNA 618
Location12q21.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-618
Ensembl geneENSG00000208022
Ensembl biotypemiRNA
Entrez693203
RNAcentralURS000075D4B4 — miRNA, 98 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385287

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385287 — 1 exons

ExonStartEnd
ENSE000015002938093573680935833

Expression profiles

Bgee: expression breadth broad, 53 present calls, max score 83.93.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017883.93gold quality
right atrium auricular regionUBERON:000663181.11gold quality
liverUBERON:000210778.18gold quality
monocyteCL:000057676.87gold quality
adult mammalian kidneyUBERON:000008275.05gold quality
heartUBERON:000094874.34gold quality
muscle layer of sigmoid colonUBERON:003580573.42gold quality
bone marrowUBERON:000237173.17gold quality
gastrocnemiusUBERON:000138873.10gold quality
kidneyUBERON:000211372.71gold quality
esophagus mucosaUBERON:000246971.93gold quality
right lobe of liverUBERON:000111471.83gold quality
left coronary arteryUBERON:000162670.31gold quality
left adrenal gland cortexUBERON:003582569.60gold quality
stomachUBERON:000094568.87gold quality
intestineUBERON:000016068.85gold quality
heart left ventricleUBERON:000208468.40gold quality
anterior cingulate cortexUBERON:000983568.19gold quality
lungUBERON:000204867.36gold quality
esophagogastric junction muscularis propriaUBERON:003584167.29gold quality
skin of legUBERON:000151166.87gold quality
lower esophagus muscularis layerUBERON:003583366.47gold quality
subcutaneous adipose tissueUBERON:000219065.91gold quality
colonUBERON:000115565.77gold quality
endocervixUBERON:000045865.76gold quality
body of uterusUBERON:000985364.94gold quality
thoracic mammary glandUBERON:000520064.91gold quality
caudate nucleusUBERON:000187364.81gold quality
amygdalaUBERON:000187664.73gold quality
spleenUBERON:000210664.62gold 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 14)

  • Implicate miR-618 in follicular lymphomagenesis, identify miR-618 as a potential risk biomarker for follicular lymphoma, and illuminate miR-618-regulated lymphomagenic pathways that can serve as therapeutic targets for follicular lymphoma. (PMID:24503492)
  • Results described a growth-suppressive role of miR-618 in TC cells partially targeting the PI3K/Akt signaling pathway. (PMID:27453421)
  • Up-regulation of miR-618 suppresses the development of plasmacytoid dendritic cells and increases their ability to secrete IFNalpha, potentially contributing to the type I IFN signature observed in systemic sclerosis patients. (PMID:28556560)
  • our study revealed that polymorphism rs2682818 in miR-618 contributes to CRC susceptibility. (PMID:29533012)
  • Circular RNA circ_0005230 was proved to be a sponge of miR-618, and expression of miR-618 could regulate CBX8 expression via targeting the 3’UTR of CBX8. (PMID:30504704)
  • miR-618 expression levels downregulated in gastric cancer (GC) tissues. In vitro miR-618 suppressed the invasion and migration capacity of GC cells. TGF-beta2 was identified and confirmed as a downstream target of miR-618. Findings suggest that miR-618 may function as a tumor suppressor in GC and suppresses metastasis in GC by negatively regulating the transcriptional level of TGF-beta2. (PMID:30737902)
  • Does miR-618 rs2682818 variant affect cancer susceptibility? Evidence from 10 case-control studies. (PMID:31383788)
  • LINC00511 was confirmed to be beneficial for osteosarcoma development via sponging miR-618 and increasing MAEL expression (PMID:31386627)
  • miR-618 rs2682818 C>A polymorphism decreases Hirschsprung disease risk in Chinese children. (PMID:32364585)
  • Circulating miR-618 Has Prognostic Significance in Patients with Metastatic Colon Cancer. (PMID:33804070)
  • Polymorphism rs2682818 participates in the progression of colorectal carcinoma via miR-618-TIMP1 regulatory axis. (PMID:34848810)
  • Exosomal microRNA-618 derived from mesenchymal stem cells attenuate the progression of hepatic fibrosis by targeting Smad4. (PMID:35199612)
  • CircRNA circ-ATAD1 suppresses miR-618 maturation to participate in colorectal cancer. (PMID:35505304)
  • Correlation between the miR-618 rs2682818 C>A polymorphism and venous malformation susceptibility. (PMID:38804038)

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.