MIR6783

gene
On this page

Also known as hsa-mir-6783

Summary

MIR6783 (microRNA 6783, HGNC:50159) is a microRNA gene on chromosome 17q21.31.

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 102466734 — 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:50159
Approved symbolMIR6783
NamemicroRNA 6783
Location17q21.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6783
Ensembl geneENSG00000278223
Ensembl biotypemiRNA
Entrez102466734
RNAcentralURS000075E610 — miRNA, 64 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000619908

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000619908 — 1 exons

ExonStartEnd
ENSE000037492364493461844934681

Expression profiles

Bgee: expression breadth broad, 57 present calls, max score 93.39.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
quadriceps femorisUBERON:000137793.39gold quality
frontal cortexUBERON:000187091.38gold quality
caudate nucleusUBERON:000187391.02gold quality
cerebellar vermisUBERON:000472090.56gold quality
bone marrowUBERON:000237185.87gold quality
lymph nodeUBERON:000002982.88gold quality
monocyteCL:000057682.30gold quality
skeletal muscle tissueUBERON:000113480.75silver quality
adrenal tissueUBERON:001830378.58gold quality
myometriumUBERON:000129673.96gold quality
heartUBERON:000094873.90gold quality
bloodUBERON:000017873.21gold quality
stomachUBERON:000094572.37gold quality
right atrium auricular regionUBERON:000663171.09gold quality
kidneyUBERON:000211370.91gold quality
body of stomachUBERON:000116170.41gold quality
gastrocnemiusUBERON:000138869.66gold quality
endometriumUBERON:000129569.43gold quality
body of pancreasUBERON:000115069.01gold quality
right lobe of liverUBERON:000111468.95gold quality
pancreasUBERON:000126468.89gold quality
liverUBERON:000210768.84gold quality
lungUBERON:000204868.40gold quality
lower esophagus muscularis layerUBERON:003583368.37gold quality
heart left ventricleUBERON:000208468.24gold quality
popliteal arteryUBERON:000225067.97gold quality
left adrenal glandUBERON:000123467.94gold quality
right adrenal glandUBERON:000123367.80gold quality
body of uterusUBERON:000985367.66gold quality
hypothalamusUBERON:000189867.33gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.17

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • rescue assays proved the function of circ_0006427/miR-6783-3p/DKK1 axis in lung adenocarcinoma progression (PMID:30470570)
  • Linc01559 Served as a Potential Oncogene and Promoted Resistance of Hepatocellular Carcinoma to Oxaliplatin by Directly Sponging miR-6783-3p. (PMID:32698745)

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.