MIR6779

gene
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Also known as hsa-mir-6779

Summary

MIR6779 (microRNA 6779, HGNC:50148) is a microRNA gene on chromosome 17q12.

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 102465467 — 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:50148
Approved symbolMIR6779
NamemicroRNA 6779
Location17q12
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6779
Ensembl geneENSG00000277057
Ensembl biotypemiRNA
Entrez102465467
RNAcentralURS000075D7CB — miRNA, 64 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000617283

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000617283 — 1 exons

ExonStartEnd
ENSE000037328853891497938915042

Expression profiles

Bgee: expression breadth broad, 75 present calls, max score 82.49.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
lymph nodeUBERON:000002982.49gold quality
rectumUBERON:000105281.38gold quality
adrenal tissueUBERON:001830377.92gold quality
monocyteCL:000057676.26gold quality
bloodUBERON:000017875.85gold quality
heart left ventricleUBERON:000208472.62gold quality
muscle of legUBERON:000138372.50gold quality
heartUBERON:000094872.15gold quality
mucosa of transverse colonUBERON:000499171.43gold quality
body of pancreasUBERON:000115071.06gold quality
right lobe of liverUBERON:000111470.51gold quality
right atrium auricular regionUBERON:000663170.47gold quality
islet of LangerhansUBERON:000000670.39gold quality
tibial arteryUBERON:000761070.16gold quality
stomachUBERON:000094569.78gold quality
left coronary arteryUBERON:000162669.63gold quality
prostate glandUBERON:000236769.48gold quality
Ammon’s hornUBERON:000195469.37gold quality
body of stomachUBERON:000116169.32gold quality
endometriumUBERON:000129569.31gold quality
urinary bladderUBERON:000125568.70gold quality
ascending aortaUBERON:000149668.51gold quality
thoracic aortaUBERON:000151568.44gold quality
anterior cingulate cortexUBERON:000983568.30gold quality
fundus of stomachUBERON:000116068.20gold quality
substantia nigraUBERON:000203868.05gold quality
transverse colonUBERON:000115767.92gold quality
adenohypophysisUBERON:000219667.87gold quality
colonUBERON:000115567.81gold quality
omental fat padUBERON:001041467.64gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.08

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • circSORBS1 inhibits lung cancer progression by sponging miR-6779-5p and directly binding RUFY3 mRNA. (PMID:38915053)

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.