MIR4691

gene
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Also known as hsa-mir-4691

Summary

MIR4691 (microRNA 4691, HGNC:41796) is a microRNA gene on chromosome 11q13.2.

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 100616403 — 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:41796
Approved symbolMIR4691
NamemicroRNA 4691
Location11q13.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4691
Ensembl geneENSG00000284435
Ensembl biotypemiRNA
Entrez100616403
RNAcentralURS000075C981 — ncRNA, 85 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000583764

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000583764 — 1 exons

ExonStartEnd
ENSE000026942696803389768033981

Expression profiles

Bgee: expression breadth broad, 40 present calls, max score 82.43.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
skeletal muscle tissueUBERON:000113482.43gold quality
islet of LangerhansUBERON:000000670.37gold quality
bloodUBERON:000017869.46gold quality
right atrium auricular regionUBERON:000663169.05gold quality
minor salivary glandUBERON:000183068.94gold quality
muscle of legUBERON:000138366.56gold quality
gastrocnemiusUBERON:000138865.40gold quality
body of stomachUBERON:000116164.37gold quality
heart left ventricleUBERON:000208464.27gold quality
small intestine Peyer’s patchUBERON:000345463.04gold quality
left lobe of thyroid glandUBERON:000112061.66gold quality
endometriumUBERON:000129561.31gold quality
tibial arteryUBERON:000761060.83gold quality
anterior cingulate cortexUBERON:000983560.67gold quality
hypothalamusUBERON:000189859.63gold quality
skin of legUBERON:000151159.10gold quality
substantia nigraUBERON:000203859.08gold quality
placentaUBERON:000198758.44gold quality
esophagus mucosaUBERON:000246958.10gold quality
lower esophagus muscularis layerUBERON:003583357.78gold quality
left ovaryUBERON:000211957.23gold quality
C1 segment of cervical spinal cordUBERON:000646956.82gold quality
putamenUBERON:000187456.63gold quality
sural nerveUBERON:001548855.64silver quality
Ammon’s hornUBERON:000195454.52gold quality
brainUBERON:000095553.47gold quality
skin of abdomenUBERON:000141652.94gold quality
omental fat padUBERON:001041451.98gold quality
transverse colonUBERON:000115751.46gold quality
nucleus accumbensUBERON:000188251.01gold 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 1)

  • TPRG1-AS1 induces RBM24 expression and inhibits liver cancer progression by sponging miR-4691-5p and miR-3659. (PMID:34328265)

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.