MIR6797

gene
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Also known as hsa-mir-6797

Summary

MIR6797 (microRNA 6797, HGNC:50169) is a microRNA gene on chromosome 19q13.2.

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 102465478 — 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:50169
Approved symbolMIR6797
NamemicroRNA 6797
Location19q13.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6797
Ensembl geneENSG00000276926
Ensembl biotypemiRNA
Entrez102465478
RNAcentralURS000075A421 — ncRNA, 72 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000621706

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000621706 — 1 exons

ExonStartEnd
ENSE000037290174186962741869698

Expression profiles

Bgee: expression breadth ubiquitous, 108 present calls, max score 97.55.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548897.55gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099191.64gold quality
adrenal tissueUBERON:001830386.14gold quality
granulocyteCL:000009485.38gold quality
right uterine tubeUBERON:000130284.46gold quality
lower esophagus mucosaUBERON:003583484.28gold quality
duodenumUBERON:000211483.78gold quality
bone marrowUBERON:000237182.56gold quality
placentaUBERON:000198779.92gold quality
bloodUBERON:000017879.78gold quality
vaginaUBERON:000099678.88gold quality
endocervixUBERON:000045878.53gold quality
monocyteCL:000057678.44gold quality
liverUBERON:000210777.41gold quality
left ovaryUBERON:000211977.25gold quality
right lobe of liverUBERON:000111477.24gold quality
ovaryUBERON:000099277.12gold quality
esophagus mucosaUBERON:000246977.01gold quality
lymph nodeUBERON:000002977.00gold quality
omental fat padUBERON:001041476.95gold quality
prostate glandUBERON:000236776.79gold quality
right ovaryUBERON:000211876.60gold quality
mucosa of transverse colonUBERON:000499176.49gold quality
skin of abdomenUBERON:000141675.97gold quality
saliva-secreting glandUBERON:000104475.50gold quality
heart left ventricleUBERON:000208475.46gold quality
esophagusUBERON:000104375.41gold quality
prefrontal cortexUBERON:000045175.38gold quality
minor salivary glandUBERON:000183075.24gold quality
gastrocnemiusUBERON:000138875.15gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.48

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Thus, PTH stimulated the expression of lnc-SUPT3H-1:16, miR-6797-5p and Runx2, and due to the sponging mechanism of lnc- SUPT3H-1:16 towards miR-6797-5p, Runx2 was protected, resulting in the promotion of osteoblast differentiation. (PMID:30562548)

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.