MIR4796

gene
On this page

Also known as hsa-mir-4796

Summary

MIR4796 (microRNA 4796, HGNC:41779) is a microRNA gene on chromosome 3q13.31.

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 100616166 — 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:41779
Approved symbolMIR4796
NamemicroRNA 4796
Location3q13.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4796
Ensembl geneENSG00000264623
Ensembl biotypemiRNA
Entrez100616166
RNAcentralURS000075A67E — miRNA, 81 nt, 4 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000580742

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000580742 — 1 exons

ExonStartEnd
ENSE00002723642114743445114743525

Expression profiles

Bgee: expression breadth broad, 61 present calls, max score 86.24.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370186.24gold quality
kidneyUBERON:000211384.02gold quality
corpus callosumUBERON:000233683.89gold quality
liverUBERON:000210783.72gold quality
adult mammalian kidneyUBERON:000008280.35gold quality
bloodUBERON:000017880.25gold quality
adrenal tissueUBERON:001830377.98gold quality
endometriumUBERON:000129577.03gold quality
monocyteCL:000057676.07gold quality
islet of LangerhansUBERON:000000672.77gold quality
gastrocnemiusUBERON:000138871.67gold quality
stomachUBERON:000094571.47gold quality
heartUBERON:000094869.43gold quality
heart left ventricleUBERON:000208468.78gold quality
esophagogastric junction muscularis propriaUBERON:003584167.92gold quality
body of pancreasUBERON:000115067.84gold quality
transverse colonUBERON:000115767.04gold quality
ascending aortaUBERON:000149666.76gold quality
right lobe of thyroid glandUBERON:000111966.41gold quality
intestineUBERON:000016065.97gold quality
tibial arteryUBERON:000761065.57gold quality
lower esophagus muscularis layerUBERON:003583365.11gold quality
descending thoracic aortaUBERON:000234564.96gold quality
skin of legUBERON:000151164.71gold quality
skin of abdomenUBERON:000141664.64gold quality
subcutaneous adipose tissueUBERON:000219064.64gold quality
right lobe of liverUBERON:000111464.58gold quality
omental fat padUBERON:001041464.24gold quality
colonUBERON:000115564.22gold quality
muscle layer of sigmoid colonUBERON:003580564.15gold 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)

  • miR-4796 enhances the sensitivity of breast cancer cells to ionising radiation by impairing the DNA repair pathway. (PMID:37460775)

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.