MIR3680-1

gene
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Also known as hsa-mir-3680

Summary

MIR3680-1 (microRNA 3680-1, HGNC:38989) is a microRNA gene on chromosome 16p12.2.

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 100500917 — 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:38989
Approved symbolMIR3680-1
NamemicroRNA 3680-1
Location16p12.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3680
Ensembl geneENSG00000265462
Ensembl biotypemiRNA
Entrez100500917
RNAcentralURS000075CE98 — ncRNA, 87 nt, 4 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000581433

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000581433 — 1 exons

ExonStartEnd
ENSE000027042702150604921506135

Expression profiles

Bgee: expression breadth ubiquitous, 105 present calls, max score 79.08.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099179.08gold quality
skeletal muscle tissueUBERON:000113477.79gold quality
adrenal tissueUBERON:001830376.79gold quality
bone marrowUBERON:000237176.66gold quality
vermiform appendixUBERON:000115473.26gold quality
bloodUBERON:000017872.69gold quality
muscle of legUBERON:000138371.14gold quality
placentaUBERON:000198771.09gold quality
monocyteCL:000057671.01gold quality
gastrocnemiusUBERON:000138870.59gold quality
sural nerveUBERON:001548870.10gold quality
apex of heartUBERON:000209869.98gold quality
corpus callosumUBERON:000233668.90gold quality
fundus of stomachUBERON:000116068.21gold quality
lymph nodeUBERON:000002967.75gold quality
smooth muscle tissueUBERON:000113567.34gold quality
liverUBERON:000210767.33gold quality
right coronary arteryUBERON:000162566.60gold quality
stomachUBERON:000094566.16gold quality
heartUBERON:000094866.13gold quality
endometriumUBERON:000129566.03gold quality
heart left ventricleUBERON:000208465.95gold quality
islet of LangerhansUBERON:000000665.79gold quality
popliteal arteryUBERON:000225065.39gold quality
rectumUBERON:000105265.34gold quality
tibial arteryUBERON:000761065.31gold quality
left coronary arteryUBERON:000162665.17gold quality
body of stomachUBERON:000116165.04gold quality
right atrium auricular regionUBERON:000663165.04gold quality
tonsilUBERON:000237265.03gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.30

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • In this study, miR-3680-5p was associated with parathyroid hormone regulation (PMID:28152049)
  • Downregulation of miR-3680-3p inhibits the progression of osteoarthritis via targeting OGG1. (PMID:35092863)

Cross-species orthologs

0 orthologs

Paralogs (1): MIR3680-2 (ENSG00000266758)

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.