MIR3914-1

gene
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Also known as hsa-mir-3914-1

Summary

MIR3914-1 (microRNA 3914-1, HGNC:38993) is a microRNA gene on chromosome 7q11.22.

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 100500836 — 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:38993
Approved symbolMIR3914-1
NamemicroRNA 3914-1
Location7q11.22
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3914-1
Ensembl geneENSG00000265878
Ensembl biotypemiRNA
Entrez100500836
RNAcentralURS000075A34C — miRNA, 99 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000584357

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000584357 — 1 exons

ExonStartEnd
ENSE000027085597130767271307770

Expression profiles

Bgee: expression breadth broad, 45 present calls, max score 96.05.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548896.05gold quality
monocyteCL:000057681.67gold quality
endometriumUBERON:000129576.29gold quality
bloodUBERON:000017874.26gold quality
stomachUBERON:000094573.37gold quality
tibial arteryUBERON:000761072.61gold quality
kidneyUBERON:000211371.83gold quality
ascending aortaUBERON:000149671.59gold quality
esophagogastric junction muscularis propriaUBERON:003584171.14gold quality
putamenUBERON:000187470.85gold quality
muscle layer of sigmoid colonUBERON:003580570.75gold quality
calcaneal tendonUBERON:000370169.63gold quality
nucleus accumbensUBERON:000188269.57gold quality
heartUBERON:000094869.55gold quality
vaginaUBERON:000099669.36gold quality
omental fat padUBERON:001041468.96gold quality
anterior cingulate cortexUBERON:000983568.74gold quality
lungUBERON:000204868.52gold quality
hypothalamusUBERON:000189867.53gold quality
tibial nerveUBERON:000132367.49gold quality
intestineUBERON:000016067.09gold quality
colonUBERON:000115567.00gold quality
right adrenal glandUBERON:000123366.60gold quality
left adrenal glandUBERON:000123466.44gold quality
myometriumUBERON:000129666.29gold quality
lower esophagus muscularis layerUBERON:003583365.68gold quality
right hemisphere of cerebellumUBERON:001489065.67gold quality
corpus callosumUBERON:000233665.52gold quality
Ammon’s hornUBERON:000195465.43gold quality
right frontal lobeUBERON:000281064.91gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.40

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta. (PMID:33672174)

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.