MIR617

gene
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Also known as hsa-mir-617

Summary

MIR617 (microRNA 617, HGNC:32873) is a microRNA gene on chromosome 12q21.31.

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 693202 — 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:32873
Approved symbolMIR617
NamemicroRNA 617
Location12q21.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-617
Ensembl geneENSG00000207763
Ensembl biotypemiRNA
OMIM621190
Entrez693202
RNAcentralURS000075D960 — miRNA, 97 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385030

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385030 — 1 exons

ExonStartEnd
ENSE000015000378083253380832629

Expression profiles

Bgee: expression breadth broad, 49 present calls, max score 84.70.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017884.70gold quality
liverUBERON:000210782.11gold quality
endometriumUBERON:000129576.60gold quality
adrenal tissueUBERON:001830375.99gold quality
heartUBERON:000094875.88gold quality
lymph nodeUBERON:000002975.68gold quality
gastrocnemiusUBERON:000138875.33gold quality
bone marrowUBERON:000237174.53gold quality
monocyteCL:000057674.14gold quality
stomachUBERON:000094572.81gold quality
kidneyUBERON:000211371.63gold quality
intestineUBERON:000016071.55gold quality
calcaneal tendonUBERON:000370171.00gold quality
lungUBERON:000204869.72gold quality
skin of legUBERON:000151169.11gold quality
esophagogastric junction muscularis propriaUBERON:003584168.99gold quality
right atrium auricular regionUBERON:000663168.47gold quality
myometriumUBERON:000129667.74gold quality
Ammon’s hornUBERON:000195467.53gold quality
minor salivary glandUBERON:000183066.39gold quality
tibial arteryUBERON:000761066.35gold quality
left adrenal gland cortexUBERON:003582566.23gold quality
lower esophagus muscularis layerUBERON:003583365.57gold quality
ascending aortaUBERON:000149665.52gold quality
anterior cingulate cortexUBERON:000983565.15gold quality
subcutaneous adipose tissueUBERON:000219064.93gold quality
caudate nucleusUBERON:000187364.91gold quality
tibial nerveUBERON:000132364.77gold quality
left lobe of thyroid glandUBERON:000112064.75gold quality
omental fat padUBERON:001041464.43gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.99

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • miR-617 Promotes the Growth of IL-22-Stimulated Keratinocytes Through Regulating FOXO4 Expression. (PMID:33211221)
  • MicroRNA 617 Targeting SERPINE1 Inhibited the Progression of Oral Squamous Cell Carcinoma. (PMID:33820852)

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.