MIR6775

gene
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Also known as hsa-mir-6775

Summary

MIR6775 (microRNA 6775, HGNC:50100) is a microRNA gene on chromosome 16q24.2.

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 102465464 — 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:50100
Approved symbolMIR6775
NamemicroRNA 6775
Location16q24.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6775
Ensembl geneENSG00000278598
Ensembl biotypemiRNA
Entrez102465464
RNAcentralURS000075DEA5 — ncRNA, 69 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000617557

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000617557 — 1 exons

ExonStartEnd
ENSE000037389438783459287834660

Expression profiles

Bgee: expression breadth broad, 94 present calls, max score 87.17.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bone marrowUBERON:000237187.17gold quality
myometriumUBERON:000129686.35gold quality
monocyteCL:000057685.57gold quality
vermiform appendixUBERON:000115484.10gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.34gold quality
gall bladderUBERON:000211077.37gold quality
mucosa of stomachUBERON:000119976.24gold quality
olfactory segment of nasal mucosaUBERON:000538676.00gold quality
muscle of legUBERON:000138375.72gold quality
gastrocnemiusUBERON:000138875.54gold quality
bloodUBERON:000017874.93gold quality
lymph nodeUBERON:000002974.42gold quality
fundus of stomachUBERON:000116074.09gold quality
placentaUBERON:000198773.87gold quality
C1 segment of cervical spinal cordUBERON:000646973.39gold quality
body of stomachUBERON:000116172.74gold quality
islet of LangerhansUBERON:000000672.61gold quality
stomachUBERON:000094572.51gold quality
lower esophagus mucosaUBERON:003583472.49gold quality
right lobe of liverUBERON:000111472.04gold quality
right frontal lobeUBERON:000281071.84gold quality
frontal cortexUBERON:000187071.65gold quality
adenohypophysisUBERON:000219671.39gold quality
esophagus mucosaUBERON:000246971.15gold quality
substantia nigraUBERON:000203871.01gold quality
prefrontal cortexUBERON:000045170.98gold quality
right atrium auricular regionUBERON:000663170.96gold quality
liverUBERON:000210770.76gold quality
Ammon’s hornUBERON:000195470.72gold quality
esophagusUBERON:000104370.51gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.03

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Tumor suppressive miR-6775-3p inhibits esophageal squamous cell carcinoma progression through forming a positive feedback loop with p53 via MAGE-A family proteins. (PMID:30333480)

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.