MIR6855

gene
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Also known as hsa-mir-6855

Summary

MIR6855 (microRNA 6855, HGNC:50061) is a microRNA gene on chromosome 9q34.11.

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 102466750 — 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:50061
Approved symbolMIR6855
NamemicroRNA 6855
Location9q34.11
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6855
Ensembl geneENSG00000276124
Ensembl biotypemiRNA
Entrez102466750
RNAcentralURS0000759BC7 — ncRNA, 67 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000622178

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000622178 — 1 exons

ExonStartEnd
ENSE00003744495129869605129869671

Expression profiles

Bgee: expression breadth broad, 98 present calls, max score 97.27.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548897.27gold quality
skeletal muscle tissueUBERON:000113489.72gold quality
vermiform appendixUBERON:000115484.19gold quality
bone marrowUBERON:000237181.92gold quality
placentaUBERON:000198779.18gold quality
adrenal tissueUBERON:001830377.96gold quality
bloodUBERON:000017876.62gold quality
muscle of legUBERON:000138375.33gold quality
calcaneal tendonUBERON:000370174.97gold quality
gastrocnemiusUBERON:000138874.74gold quality
monocyteCL:000057673.56gold quality
lymph nodeUBERON:000002973.33gold quality
heart left ventricleUBERON:000208472.63gold quality
fundus of stomachUBERON:000116072.58gold quality
right ovaryUBERON:000211872.48gold quality
granulocyteCL:000009472.43gold quality
endometriumUBERON:000129571.80gold quality
tibial arteryUBERON:000761071.62gold quality
popliteal arteryUBERON:000225071.56gold quality
heartUBERON:000094871.49gold quality
ectocervixUBERON:001224971.49gold quality
islet of LangerhansUBERON:000000671.12gold quality
smooth muscle tissueUBERON:000113570.83gold quality
right atrium auricular regionUBERON:000663170.82gold quality
thoracic aortaUBERON:000151570.56gold quality
ascending aortaUBERON:000149670.55gold quality
stomachUBERON:000094570.48gold quality
right adrenal glandUBERON:000123370.48gold quality
ovaryUBERON:000099270.46gold quality
body of pancreasUBERON:000115070.28gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.22

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • The role of the redox/miR-6855-3p/PRDX5A axis in reversing SLUG-mediated BRCA2 silencing in breast cancer cells. (PMID:31987042)

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.