MIR6826

gene
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Also known as hsa-mir-6826

Summary

MIR6826 (microRNA 6826, HGNC:50001) 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 102465496 — 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:50001
Approved symbolMIR6826
NamemicroRNA 6826
Location3q21.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6826
Ensembl geneENSG00000278658
Ensembl biotypemiRNA
Entrez102465496
RNAcentralURS000075CF9E — miRNA, 98 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000617808

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000617808 — 1 exons

ExonStartEnd
ENSE00003737241129272146129272243

Expression profiles

Bgee: expression breadth broad, 92 present calls, max score 78.22.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370178.22gold quality
monocyteCL:000057677.87gold quality
fundus of stomachUBERON:000116077.59gold quality
bone marrowUBERON:000237176.92gold quality
adrenal tissueUBERON:001830376.35gold quality
bloodUBERON:000017875.29gold quality
ectocervixUBERON:001224974.14gold quality
body of pancreasUBERON:000115072.91gold quality
gastrocnemiusUBERON:000138872.72gold quality
smooth muscle tissueUBERON:000113571.95gold quality
liverUBERON:000210771.86gold quality
stomachUBERON:000094571.49gold quality
islet of LangerhansUBERON:000000671.18gold quality
prefrontal cortexUBERON:000045171.12gold quality
ascending aortaUBERON:000149671.03gold quality
thoracic aortaUBERON:000151571.03gold quality
right lobe of liverUBERON:000111470.76gold quality
endometriumUBERON:000129570.62gold quality
body of stomachUBERON:000116170.61gold quality
left coronary arteryUBERON:000162670.24gold quality
tibial arteryUBERON:000761070.19gold quality
popliteal arteryUBERON:000225070.16gold quality
right ovaryUBERON:000211869.88gold quality
heart left ventricleUBERON:000208469.73gold quality
heartUBERON:000094869.60gold quality
left ovaryUBERON:000211969.27gold quality
body of uterusUBERON:000985369.18gold quality
myometriumUBERON:000129669.09gold quality
left uterine tubeUBERON:000130368.90gold quality
Brodmann (1909) area 9UBERON:001354068.80gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.30

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Although further clarification is needed regarding the functions of miR-6826 and miR-6875 and their relationship to immunerelated molecules, plasma miR-6826 and miR-6875 may be useful negative biomarkers for predicting the efficacy of vaccine treatment in colorectal cancer. (PMID:27878288)

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.