MIR4465

gene
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Also known as hsa-mir-4465

Summary

MIR4465 (microRNA 4465, HGNC:41842) is a microRNA gene on chromosome 6q24.1.

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 100616180 — 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:41842
Approved symbolMIR4465
NamemicroRNA 4465
Location6q24.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4465
Ensembl geneENSG00000264390
Ensembl biotypemiRNA
Entrez100616180
RNAcentralURS000075EA2C — miRNA, 70 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000583434

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000583434 — 1 exons

ExonStartEnd
ENSE00002713435140683814140683883

Expression profiles

Bgee: expression breadth broad, 12 present calls, max score 72.19.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
gastrocnemiusUBERON:000138872.19gold quality
calcaneal tendonUBERON:000370171.16gold quality
lower esophagus muscularis layerUBERON:003583368.63gold quality
upper lobe of left lungUBERON:000895268.31gold quality
left adrenal glandUBERON:000123468.00gold quality
left ovaryUBERON:000211964.52gold quality
ascending aortaUBERON:000149663.93gold quality
thyroid glandUBERON:000204663.65gold quality
left lobe of thyroid glandUBERON:000112063.42gold quality
tibial nerveUBERON:000132362.97gold quality
esophagus mucosaUBERON:000246962.73gold quality
left testisUBERON:000453343.32gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.14

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 6)

  • miR-4465 significantly inhibited the expression of PTEN, upregulated phosphorylated AKT, and thereby inhibited autophagy by activating mTOR. (PMID:30421325)
  • LncRNA SDHAP1 confers paclitaxel resistance of ovarian cancer by regulating EIF4G2 expression via miR-4465. (PMID:32211849)
  • HDAC7 promotes the oncogenicity of nasopharyngeal carcinoma cells by miR-4465-EphA2 signaling axis. (PMID:32376822)
  • Expression level of VLDL receptor and VLDL-c levels in the malignant and benign breast tumors: The correlation with miRNA-4465 and miRNA-1297. (PMID:32711022)
  • LINC00240 sponges miR-4465 to promote proliferation, migration, and invasion of hepatocellular carcinoma cells via HGF/c-MET signaling pathway. (PMID:33155201)
  • MiR-4465-modified mesenchymal stem cell-derived small extracellular vesicles inhibit liver fibrosis development via targeting LOXL2 expression. (PMID:39011679)

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.