MIR6825

gene
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Also known as hsa-mir-6825

Summary

MIR6825 (microRNA 6825, HGNC:50208) is a microRNA gene on chromosome 3q21.3.

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 102466199 — 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:50208
Approved symbolMIR6825
NamemicroRNA 6825
Location3q21.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6825
Ensembl geneENSG00000275067
Ensembl biotypemiRNA
Entrez102466199
RNAcentralURS000075B4D3 — miRNA, 66 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000618505

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000618505 — 1 exons

ExonStartEnd
ENSE00003748134127575266127575331

Expression profiles

Bgee: expression breadth broad, 84 present calls, max score 86.29.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830386.29gold quality
prefrontal cortexUBERON:000045183.04gold quality
sural nerveUBERON:001548880.48gold quality
lower esophagus mucosaUBERON:003583476.45gold quality
muscle of legUBERON:000138375.45gold quality
bloodUBERON:000017875.25gold quality
placentaUBERON:000198774.03gold quality
gastrocnemiusUBERON:000138873.55gold quality
adult mammalian kidneyUBERON:000008272.94gold quality
granulocyteCL:000009472.55gold quality
monocyteCL:000057671.80gold quality
endocervixUBERON:000045871.68gold quality
heart left ventricleUBERON:000208471.55gold quality
left coronary arteryUBERON:000162670.81gold quality
heartUBERON:000094870.30gold quality
body of stomachUBERON:000116169.76gold quality
adrenal glandUBERON:000236969.76gold quality
tibial arteryUBERON:000761069.60gold quality
popliteal arteryUBERON:000225069.56gold quality
fundus of stomachUBERON:000116069.24gold quality
amygdalaUBERON:000187669.08gold quality
left adrenal gland cortexUBERON:003582569.06gold quality
myometriumUBERON:000129669.04gold quality
left ovaryUBERON:000211968.91gold quality
body of pancreasUBERON:000115068.56gold quality
right lobe of liverUBERON:000111468.46gold quality
right atrium auricular regionUBERON:000663168.45gold quality
kidneyUBERON:000211368.43gold quality
lower esophagus muscularis layerUBERON:003583368.03gold quality
right hemisphere of cerebellumUBERON:001489067.98gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.15

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Exosome-derived lnc-HOXB8-1:2 induces tumor-associated macrophage infiltration to promote neuroendocrine differentiated colorectal cancer progression by sponging hsa-miR-6825-5p. (PMID:36030223)

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.