MIR6803

gene
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Also known as hsa-mir-6803

Summary

MIR6803 (microRNA 6803, HGNC:50035) is a microRNA gene on chromosome 19q13.42.

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 102466739 — 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:50035
Approved symbolMIR6803
NamemicroRNA 6803
Location19q13.42
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6803
Ensembl geneENSG00000278264
Ensembl biotypemiRNA
Entrez102466739
RNAcentralURS000075BF8E — miRNA, 65 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000615997

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000615997 — 1 exons

ExonStartEnd
ENSE000037308135524518655245250

Expression profiles

Bgee: expression breadth broad, 60 present calls, max score 93.69.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548893.69gold quality
lymph nodeUBERON:000002981.34gold quality
bone marrowUBERON:000237180.17gold quality
bloodUBERON:000017876.35gold quality
placentaUBERON:000198775.90gold quality
prefrontal cortexUBERON:000045172.93gold quality
C1 segment of cervical spinal cordUBERON:000646972.91gold quality
heartUBERON:000094872.63gold quality
heart left ventricleUBERON:000208472.06gold quality
stomachUBERON:000094569.31gold quality
right lobe of liverUBERON:000111469.16gold quality
vaginaUBERON:000099669.04gold quality
right atrium auricular regionUBERON:000663168.85gold quality
tibial arteryUBERON:000761068.72gold quality
Ammon’s hornUBERON:000195468.53gold quality
ascending aortaUBERON:000149668.49gold quality
body of stomachUBERON:000116168.31gold quality
tibial nerveUBERON:000132368.22gold quality
caudate nucleusUBERON:000187367.93gold quality
left adrenal gland cortexUBERON:003582567.63gold quality
left adrenal glandUBERON:000123467.61gold quality
endometriumUBERON:000129567.59gold quality
omental fat padUBERON:001041467.31gold quality
transverse colonUBERON:000115767.27gold quality
esophagus mucosaUBERON:000246967.11gold quality
lower esophagus muscularis layerUBERON:003583366.64gold quality
putamenUBERON:000187466.27gold quality
right adrenal glandUBERON:000123365.70gold quality
right frontal lobeUBERON:000281065.58gold quality
spleenUBERON:000210665.46gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.12

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Cox regression analysis revealed high levels of exosomal miR-6803-5p was associated with poor prognosis in colorectal cancer (CRC) independent of other confounding factors. Thus, exosomal miR-6803-5p is a potential diagnostic and prognostic biomarker for patients with CRC. (PMID:29240249)

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.