MIR3713

gene
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Also known as hsa-mir-3713

Summary

MIR3713 (microRNA 3713, HGNC:38926) is a microRNA gene on chromosome 15q24.3.

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 100500855 — 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:38926
Approved symbolMIR3713
NamemicroRNA 3713
Location15q24.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3713
Ensembl geneENSG00000266449
Ensembl biotypemiRNA
Entrez100500855
RNAcentralURS000075CF19 — ncRNA, 45 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000581359

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000581359 — 1 exons

ExonStartEnd
ENSE000027144587658664776586691

Expression profiles

Bgee: expression breadth broad, 39 present calls, max score 81.41.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017881.41gold quality
kidneyUBERON:000211380.95gold quality
dorsolateral prefrontal cortexUBERON:000983474.86gold quality
gastrocnemiusUBERON:000138874.76gold quality
adrenal tissueUBERON:001830374.32gold quality
intestineUBERON:000016074.21gold quality
monocyteCL:000057673.99gold quality
body of stomachUBERON:000116173.66gold quality
liverUBERON:000210773.23gold quality
endometriumUBERON:000129571.35gold quality
anterior cingulate cortexUBERON:000983571.19gold quality
right atrium auricular regionUBERON:000663171.04gold quality
lower esophagus muscularis layerUBERON:003583370.96gold quality
stomachUBERON:000094570.66gold quality
body of pancreasUBERON:000115070.33gold quality
tibial arteryUBERON:000761070.05gold quality
esophagogastric junction muscularis propriaUBERON:003584169.85gold quality
prostate glandUBERON:000236769.52gold quality
tibial nerveUBERON:000132369.43gold quality
ascending aortaUBERON:000149669.41gold quality
skin of legUBERON:000151169.21gold quality
subcutaneous adipose tissueUBERON:000219068.39gold quality
esophagus mucosaUBERON:000246968.33gold quality
caudate nucleusUBERON:000187368.07gold quality
muscle layer of sigmoid colonUBERON:003580568.04gold quality
colonUBERON:000115567.69gold quality
left ovaryUBERON:000211967.31gold quality
spleenUBERON:000210666.94gold quality
putamenUBERON:000187466.80gold quality
omental fat padUBERON:001041465.95gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.97

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • The effects of miR-3713 on Transitional cell carcinoma (TCC) cell growth appeared to result from its modification of MMP9 levels, in which miR-3713 was found to bind to the 3’-UTR of MMP9 mRNA to inhibit its protein translation in TCC cells (PMID:27577949)

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.