MIR513C

gene
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Also known as hsa-mir-513c

Summary

MIR513C (microRNA 513c, HGNC:33934) is a microRNA gene on chromosome Xq27.3.

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 100302114 — 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:33934
Approved symbolMIR513C
NamemicroRNA 513c
LocationXq27.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-513c
Ensembl geneENSG00000216171
Ensembl biotypemiRNA
Entrez100302114
RNAcentralURS000075A3A1 — miRNA, 84 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000401352

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000401352 — 1 exons

ExonStartEnd
ENSE00001808341147189704147189787

Expression profiles

Bgee: expression breadth broad, 12 present calls, max score 79.37.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adult mammalian kidneyUBERON:000008279.37gold quality
bloodUBERON:000017875.47gold quality
right lobe of liverUBERON:000111468.62gold quality
small intestineUBERON:000210866.87gold quality
transverse colonUBERON:000115764.74gold quality
small intestine Peyer’s patchUBERON:000345464.59gold quality
left ovaryUBERON:000211963.27gold quality
vaginaUBERON:000099663.16gold quality
right frontal lobeUBERON:000281054.88gold quality
left testisUBERON:000453342.36gold quality
testisUBERON:000047341.92gold quality
right testisUBERON:000453439.74gold 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 7)

  • miR513c functions as a tumor suppressor miRNA, mediated predominantly through the direct suppression of the expression of LRP6. (PMID:26063413)
  • Overexpression of miR-513c suppresses neuroblastoma cells’ migration, invasion, and proliferation. We demonstrate the glutaminase (GLS) is a direct target of miR-513c in human neuroblastoma cells. (PMID:28800318)
  • Low expression of MIR513C due to LncRNA FLVCR1-AS1 sponge is associated with migration, and invasion in hepatocellular carcinoma. (PMID:29574975)
  • Results show that miR-513c directly targets TCF7. Its expression is regulated by LOC728196 which acts as the sponge for miR-513c to upregulate TCF7 expression in glioma cells. (PMID:30179681)
  • MicroRNA-513c-5p is involved in the pathogenesis of preeclampsia by regulating of low-density lipoprotein receptor-associated protein 6. (PMID:34930169)
  • hsa-miR-424-5p and hsa-miR-513c-3p dysregulation mediated by IFN-gamma is associated with salivary gland dysfunction in Sjogren’s syndrome patients. (PMID:37229808)
  • lncRNA SEMA3B-AS1 Inhibits miR-513c-5p to Regulate the Progression of Triple-negative Breast Cancer. (PMID:38030196)

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.