MIR517C

gene
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Also known as hsa-mir-517c

Summary

MIR517C (microRNA 517c, HGNC:32124) is a microRNA gene on chromosome 19q13.42.

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 574492 — 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:32124
Approved symbolMIR517C
NamemicroRNA 517c
Location19q13.42
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-517c
Ensembl geneENSG00000207838
Ensembl biotypemiRNA
OMIM620621
Entrez574492
RNAcentralURS0000759A4A — miRNA, 95 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385103

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385103 — 1 exons

ExonStartEnd
ENSE000015001095374131353741407

Expression profiles

Bgee: expression breadth broad, 18 present calls, max score 75.13.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017875.13gold quality
monocyteCL:000057674.04gold quality
calcaneal tendonUBERON:000370171.67gold quality
lungUBERON:000204871.12gold quality
ascending aortaUBERON:000149670.17gold quality
transverse colonUBERON:000115769.49gold quality
lower esophagus muscularis layerUBERON:003583368.99gold quality
esophagus mucosaUBERON:000246968.45gold quality
body of stomachUBERON:000116168.38gold quality
subcutaneous adipose tissueUBERON:000219064.72gold quality
endocervixUBERON:000045864.26gold quality
dorsolateral prefrontal cortexUBERON:000983463.70gold quality
pituitary glandUBERON:000000762.24gold quality
spleenUBERON:000210660.50gold quality
renal glomerulusUBERON:000007460.43gold quality
placentaUBERON:000198752.77gold quality
right frontal lobeUBERON:000281051.22gold quality
left testisUBERON:000453344.11gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.49

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 5)

  • data implicate miR-517c and 520g as oncogenes and promising biological markers for CNS-PNET and provide important insights into oncogenic properties of the C19MC locus (PMID:19962671)
  • Down-regulation of both miR-517a and miR-517c contribute to hepatocellular carcinoma cells development through regulating Pyk2. (PMID:23142219)
  • MiR-517c overexpression increased expression of the anti-angiogenic protein, sFLT1. (PMID:25799546)
  • provided support for a link between autophagy and epithelial-to-mesenchymal (-like) transition status in WT TP53 GBM cells and provided evidence for the signaling pathway (MIR517C-KPNA2-cytoplasmic TP53) involved in attenuating autophagy (PMID:26553592)
  • MiR-517-5p is highly expressed in placental samples of preeclampsia pregnancies, which could promote proliferative and invasive abilities of cells by inhibiting ERK/MMP-2 pathway. (PMID:30402831)

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.