MIR1914

gene
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Also known as hsa-mir-1914

Summary

MIR1914 (microRNA 1914, HGNC:35398) is a microRNA gene on chromosome 20q13.33.

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 100302137 — 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:35398
Approved symbolMIR1914
NamemicroRNA 1914
Location20q13.33
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1914
Ensembl geneENSG00000284433
Ensembl biotypemiRNA
Entrez100302137
RNAcentralURS000075A6FE — miRNA, 80 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000607800

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000607800 — 1 exons

ExonStartEnd
ENSE000037021376394146563941544

Expression profiles

Bgee: expression breadth broad, 22 present calls, max score 92.51.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
heart left ventricleUBERON:000208492.51gold quality
anterior cingulate cortexUBERON:000983585.23gold quality
stomachUBERON:000094582.11gold quality
skeletal muscle tissueUBERON:000113481.22gold quality
myometriumUBERON:000129676.81gold quality
C1 segment of cervical spinal cordUBERON:000646976.04gold quality
colonUBERON:000115574.89gold quality
hypothalamusUBERON:000189873.16gold quality
lower esophagus muscularis layerUBERON:003583370.33gold quality
muscle of legUBERON:000138369.77gold quality
nucleus accumbensUBERON:000188269.29gold quality
leukocyteCL:000073868.37gold quality
prostate glandUBERON:000236768.16gold quality
Ammon’s hornUBERON:000195467.85gold quality
bloodUBERON:000017867.73gold quality
right atrium auricular regionUBERON:000663166.15gold quality
gastrocnemiusUBERON:000138863.88gold quality
skin of legUBERON:000151161.68gold quality
dorsolateral prefrontal cortexUBERON:000983458.16gold quality
small intestineUBERON:000210856.13gold quality
caudate nucleusUBERON:000187354.36gold quality
subcutaneous adipose tissueUBERON:000219053.74gold 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 4)

  • miR-647 and miR-1914 promote the proliferation and migration equivalently by downregulating NFIX in CRC cells in vitro. (PMID:28990086)
  • microRNA-1914, which is regulated by lncRNA DUXAP10, inhibits cell proliferation by targeting the GPR39-mediated PI3K/AKT/mTOR pathway in HCC. (PMID:31576658)
  • The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration. (PMID:33907947)
  • Monocyte-Derived miRNA-1914-5p Attenuates IL-1beta-Induced Monocyte Adhesion and Transmigration. (PMID:36769149)

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.