MIR6867

gene
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Also known as hsa-mir-6867

Summary

MIR6867 (microRNA 6867, HGNC:50134) is a microRNA gene on chromosome 17q21.1.

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 102465523 — 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:50134
Approved symbolMIR6867
NamemicroRNA 6867
Location17q21.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6867
Ensembl geneENSG00000274621
Ensembl biotypemiRNA
Entrez102465523
RNAcentralURS000075B8A6 — miRNA, 67 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000610636

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000610636 — 1 exons

ExonStartEnd
ENSE000037509614019359740193663

Expression profiles

Bgee: expression breadth ubiquitous, 102 present calls, max score 95.55.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
lower esophagus mucosaUBERON:003583495.55gold quality
skin of legUBERON:000151192.67gold quality
zone of skinUBERON:000001491.83gold quality
skin of abdomenUBERON:000141690.92gold quality
vaginaUBERON:000099689.76gold quality
lymph nodeUBERON:000002989.32gold quality
esophagus mucosaUBERON:000246989.07gold quality
mucosa of transverse colonUBERON:000499187.94gold quality
urinary bladderUBERON:000125585.05gold quality
duodenumUBERON:000211484.89gold quality
esophagusUBERON:000104384.19gold quality
transverse colonUBERON:000115781.08gold quality
ectocervixUBERON:001224979.35gold quality
colonUBERON:000115577.76gold quality
right frontal lobeUBERON:000281077.08gold quality
bone marrowUBERON:000237177.01gold quality
frontal cortexUBERON:000187076.96gold quality
endocervixUBERON:000045876.74gold quality
tonsilUBERON:000237276.74gold quality
right hemisphere of cerebellumUBERON:001489076.56gold quality
intestineUBERON:000016076.49gold quality
kidneyUBERON:000211375.30gold quality
cerebellar hemisphereUBERON:000224575.13gold quality
hypothalamusUBERON:000189874.82gold quality
cerebral cortexUBERON:000095674.63gold quality
nucleus accumbensUBERON:000188274.61gold quality
bloodUBERON:000017874.47gold quality
dorsolateral prefrontal cortexUBERON:000983474.36gold quality
Brodmann (1909) area 9UBERON:001354074.36gold quality
muscle of legUBERON:000138374.14gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.34

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • lncRNA ARAP1-AS1 enhances proliferation and impairs apoptosis of lymphoma cells by sponging miR-6867-5p. (PMID:37599524)
  • The human PTGR1 gene expression is controlled by TE-derived Z-DNA forming sequence cooperating with miR-6867-5p. (PMID:38413664)

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.