MIR654

gene
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Also known as hsa-mir-654

Summary

MIR654 (microRNA 654, HGNC:32910) is a microRNA gene on chromosome 14q32.31.

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 724024 — 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:32910
Approved symbolMIR654
NamemicroRNA 654
Location14q32.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-654
Ensembl geneENSG00000207934
Ensembl biotypemiRNA
Entrez724024
RNAcentralURS000075B509 — miRNA, 81 nt, 17 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385199

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385199 — 1 exons

ExonStartEnd
ENSE00001500205101040219101040299

Expression profiles

Bgee: expression breadth broad, 53 present calls, max score 97.62.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830397.62gold quality
placentaUBERON:000198786.96gold quality
stomachUBERON:000094586.08gold quality
lungUBERON:000204884.83gold quality
kidneyUBERON:000211381.08gold quality
heartUBERON:000094879.72gold quality
intestineUBERON:000016079.60gold quality
adrenal glandUBERON:000236976.24gold quality
calcaneal tendonUBERON:000370176.08gold quality
liverUBERON:000210775.26gold quality
colonUBERON:000115574.18gold quality
gastrocnemiusUBERON:000138872.33gold quality
islet of LangerhansUBERON:000000671.99gold quality
substantia nigraUBERON:000203869.27gold quality
right adrenal glandUBERON:000123368.91gold quality
prefrontal cortexUBERON:000045168.69gold quality
skin of abdomenUBERON:000141668.61gold quality
body of stomachUBERON:000116168.50gold quality
endometriumUBERON:000129568.39gold quality
anterior cingulate cortexUBERON:000983568.23gold quality
Ammon’s hornUBERON:000195468.06gold quality
esophagusUBERON:000104367.42gold quality
lower esophagus muscularis layerUBERON:003583367.42gold quality
left adrenal gland cortexUBERON:003582567.10gold quality
left adrenal glandUBERON:000123466.70gold quality
omental fat padUBERON:001041466.11gold quality
adult mammalian kidneyUBERON:000008265.28gold quality
tibial arteryUBERON:000761065.07gold quality
cerebral cortexUBERON:000095665.05gold quality
muscle layer of sigmoid colonUBERON:003580564.71gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.16

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 28)

  • Mir-654-3p, mapped to the 14q32.31 locus, regulates proliferation, apoptosis, migration and invasion in metastatic prostate cancer cells. (PMID:24166498)
  • Report down-regulation of 14q32-encoded miRNA-654-3p in papillary thyroid carcinomas. (PMID:28030816)
  • Findings suggest that the miR-654-5p/GRAP/Ras/Erk signaling pathway in OSCC cells might contribute to the underlying mechanism through which miR-654-5p participates in the regulation of OSCC progression. (PMID:29364705)
  • The CircHIPK3 could promote IGF2BP3 expression via interacting with miR-654 in glioma cells. (PMID:30057315)
  • CDCP1 and PLAGL2 oncogenes were found to be the most relevant direct miR-654-5p targets and both genes convey in a molecular signature associated with key cancer pathways relevant to ovarian tumorigenesis, such as MYC, WNT and AKT pathways. This unveiled the tumor suppressor function of miR-654-5p, suggesting that its restoration or co-targeting of CDCP1 and PLAGL2 may be an effective therapeutic approach for cancer. (PMID:31278368)
  • MiRNA Regulation of MIF in SLE and Attenuation of Murine Lupus Nephritis With miR-654. (PMID:31608058)
  • Study found that miR-654 was up-regulated in gastric cancer (GC) tissues and cells, and promoted the proliferation of GC cells. miR-654 can inhibit the protein expression of p21 in GC cells, whereas circRHOBTB3 enhanced the protein expression of p21. circRHOBTB3 inhibited the activity of miR-654, and thus, reversed the miR- 654 induced cell proliferation and upregulated the protein expression of p21 indirectly. (PMID:31928527)
  • miR-654-3p predicts the prognosis of hepatocellular carcinoma and inhibits the proliferation, migration, and invasion of cancer cells. (PMID:32176631)
  • MiR-654-5p regulated cell progression and tumor growth through targeting SIRT6 in osteosarcoma. (PMID:32329825)
  • Circular RNA hsa_circ_0085131 is involved in cisplatin-resistance of non-small-cell lung cancer cells by regulating autophagy. (PMID:32449799)
  • Long noncoding RNA MKLN1AS aggravates hepatocellular carcinoma progression by functioning as a molecular sponge for miR6543p, thereby promoting hepatomaderived growth factor expression. (PMID:33000222)
  • Long intergenic noncoding RNA LINC01232 contributes to esophageal squamous cell carcinoma progression by sequestering microRNA6543p and consequently promoting hepatomaderived growth factor expression. (PMID:33125097)
  • Hsa_circ_0079480 promotes tumor progression in acute myeloid leukemia via miR-654-3p/HDGF axis. (PMID:33290265)
  • miR6543p suppresses cell viability and promotes apoptosis by targeting RASAL2 in nonsmallcell lung cancer. (PMID:33300072)
  • miR6545p inhibits autophagy by targeting ATG7 via mTOR signaling in intervertebral disc degeneration. (PMID:33846806)
  • LncRNA TP73-AS1 promotes oxidized low-density lipoprotein-induced apoptosis of endothelial cells in atherosclerosis by targeting the miR-654-3p/AKT3 axis. (PMID:34103010)
  • Interference with circRNA DOCK1 inhibits hepatocellular carcinoma cell proliferation, invasion and migration by regulating the miR-654-5p/SMAD2 axis. (PMID:34184075)
  • LINC02532 Contributes to Radiosensitivity in Clear Cell Renal Cell Carcinoma through the miR-654-5p/YY1 Axis. (PMID:34834139)
  • CircRNA CORO1C Regulates miR-654-3p/USP7 Axis to Mediate Laryngeal Squamous Cell Carcinoma Progression. (PMID:35064359)
  • EMX2OS Delays Wilms’Tumor Progression via Targeting miR-654-3p. (PMID:35181613)
  • miR-654-5p Suppresses Migration and Proliferation of Vascular Smooth Muscle Cells by Targeting ADAMTS-7. (PMID:35462367)
  • Comprehensive Analysis of hsa-miR-654-5p’s Tumor-Suppressing Functions. (PMID:35742854)
  • LncRNA NEAT1 inhibits apoptosis and autophagy of ovarian granulosa cells through miR-654/STC2-mediated MAPK signaling pathway. (PMID:36634743)
  • CircPLXNB2 regulates acute myeloid leukemia progression through miR-654-3p/CCND1 axis. (PMID:37272581)
  • MiR-654-3p targets SRC to suppress tumor growth in non-small cell lung cancer. (PMID:37329531)
  • Long noncoding RNA LINC00885 upregulates NCK1 to promote cell viability and migration of triple-negative breast cancer cells through sponging miR-654-3p. (PMID:37694355)
  • Circ_0084188 promotes colorectal cancer progression by sponging miR-654-3p and regulating kruppel-like factor 12. (PMID:37698263)
  • Circular RNA EFR3A promotes nasopharyngeal carcinoma progression through modulating the miR-654-3p/EFR3A axis. (PMID:38063110)

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.