MIR2909

gene
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Also known as hsa-mir-2909

Summary

MIR2909 (microRNA 2909, HGNC:38372) is a microRNA gene on chromosome 17q12.

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 100422969 — 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:38372
Approved symbolMIR2909
NamemicroRNA 2909
Location17q12
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-2909
Ensembl geneENSG00000276326
Ensembl biotypemiRNA
Entrez100422969
RNAcentralURS000075C656 — ncRNA, 69 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000617113

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000617113 — 1 exons

ExonStartEnd
ENSE000037487213703374537033813

Expression profiles

Bgee: expression breadth broad, 73 present calls, max score 84.97.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adult mammalian kidneyUBERON:000008284.97gold quality
calcaneal tendonUBERON:000370183.81gold quality
kidneyUBERON:000211382.72gold quality
corpus callosumUBERON:000233681.88gold quality
liverUBERON:000210779.44gold quality
bloodUBERON:000017878.36gold quality
muscle of legUBERON:000138377.87gold quality
bone marrowUBERON:000237177.71gold quality
adrenal tissueUBERON:001830376.86gold quality
monocyteCL:000057676.53gold quality
left coronary arteryUBERON:000162675.58gold quality
gastrocnemiusUBERON:000138873.94gold quality
islet of LangerhansUBERON:000000673.32gold quality
stomachUBERON:000094573.32gold quality
heartUBERON:000094871.20gold quality
body of stomachUBERON:000116169.96gold quality
body of pancreasUBERON:000115069.02gold quality
tibial arteryUBERON:000761069.01gold quality
esophagogastric junction muscularis propriaUBERON:003584168.92gold quality
Ammon’s hornUBERON:000195468.29gold quality
lungUBERON:000204868.07gold quality
right atrium auricular regionUBERON:000663167.89gold quality
body of uterusUBERON:000985367.73gold quality
heart left ventricleUBERON:000208467.27gold quality
lower esophagusUBERON:001347367.18gold quality
lower esophagus muscularis layerUBERON:003583367.14gold quality
colonUBERON:000115566.84gold quality
skin of legUBERON:000151166.82gold quality
zone of skinUBERON:000001466.74gold quality
intestineUBERON:000016066.67gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 15)

  • results suggest that miR-2909 may modulate native immunity in general and help in providing protective immunity against viral infections in particular (PMID:22504889)
  • propose that miR-2909 RNomics may be a step forward in understanding human CHD at the epigenomic level and can be exploited for designing new therapeutic strategies as well as diagnostic and prognostic markers for this disease in future (PMID:24634009)
  • This study identified a novel miR-2909-KLF4 molecular axis able to differentiate between the pathogeneses of pediatric B- and T-cell ALLs, and which may represent a new diagnostic/prognostic marker. (PMID:25037230)
  • MALT1 exerts its effect upon immune response through the initiation of cellular miR-2909 RNomics. (PMID:25500259)
  • High glucose-induced human cellular immune response is governed by miR-2909. (PMID:25616369)
  • In the face of high glucose threat, mitochondrial UCP2 gene expression is regulated by miR-2909 and AATF. (PMID:25976474)
  • High miR-2909 expression is associated with Th1 immune response coupled with effector IgA class switching thereby tailoring their immune system to ensure increased risk to infections and chronic diseases. (PMID:26302178)
  • miR-2909 could play a vital role in prostate carcinogenesis through modulation of ISGylation system and TGFbeta signalling via STAT1/SOCS3. (PMID:28622443)
  • study shows that androgen receptor and miR-2909 drives the down-regulation of TGFBR2 by acting through positive feedback loop and thereby attenuating the inhibitory effects of TGFbeta signaling (PMID:28754634)
  • Studied recruitment patterns of urinary-exosomal miR-2909 in bladder and prostate cancer and its relation to disease severity. (PMID:28764970)
  • Post-transcriptional modification, especially 3’-end adenylation and uridylation of miR-2909, exerts opposing effects that may contribute to direct its sorting into exosomes secreted by cancer cells. (PMID:29468700)
  • the role of miR-2909 in the regulation of mitochondrial function within human melanocytes, is reported. (PMID:30506863)
  • Chemical induced pathognomonic features observed in human vitiligo are mediated through miR-2909 RNomics pathway. (PMID:33039241)
  • Prediction of recurrence of non-muscle invasive bladder cancer: The role of androgen receptor and miRNA-2909. (PMID:35430138)
  • Integrative Expression, Survival Analysis and Cellular miR-2909 Molecular Interplay in MRN Complex Check Point Sensor Genes (MRN-CSG) Involved in Breast Cancer. (PMID:36220723)

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.