MIR4798

gene
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Also known as hsa-mir-4798

Summary

MIR4798 (microRNA 4798, HGNC:41616) is a microRNA gene on chromosome 4p16.1.

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 100616471 — 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:41616
Approved symbolMIR4798
NamemicroRNA 4798
Location4p16.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4798
Ensembl geneENSG00000264658
Ensembl biotypemiRNA
Entrez100616471
RNAcentralURS000075B320 — miRNA, 75 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000578126

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000578126 — 1 exons

ExonStartEnd
ENSE0000270835073104507310524

Expression profiles

Bgee: expression breadth broad, 42 present calls, max score 84.56.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370184.56gold quality
adrenal tissueUBERON:001830378.75gold quality
lungUBERON:000204876.16gold quality
monocyteCL:000057672.93gold quality
putamenUBERON:000187472.89gold quality
heart left ventricleUBERON:000208472.59gold quality
right lobe of liverUBERON:000111472.06gold quality
stomachUBERON:000094571.65gold quality
heartUBERON:000094870.81gold quality
prostate glandUBERON:000236769.72gold quality
corpus callosumUBERON:000233669.24gold quality
dorsolateral prefrontal cortexUBERON:000983468.95gold quality
esophagogastric junction muscularis propriaUBERON:003584167.63gold quality
muscle layer of sigmoid colonUBERON:003580566.30gold quality
lower esophagus muscularis layerUBERON:003583365.99gold quality
Brodmann (1909) area 9UBERON:001354065.54gold quality
substantia nigraUBERON:000203865.22gold quality
omental fat padUBERON:001041465.07gold quality
right lobe of thyroid glandUBERON:000111964.95gold quality
body of uterusUBERON:000985364.57gold quality
skin of legUBERON:000151164.10gold quality
tibial arteryUBERON:000761063.70gold quality
C1 segment of cervical spinal cordUBERON:000646963.25gold quality
skin of abdomenUBERON:000141662.90gold quality
esophagus mucosaUBERON:000246962.43gold quality
right hemisphere of cerebellumUBERON:001489062.29gold quality
right atrium auricular regionUBERON:000663162.28gold quality
tibial nerveUBERON:000132361.78gold quality
pituitary glandUBERON:000000761.58gold quality
Ammon’s hornUBERON:000195461.45gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.33

Regulation

Is transcription factor: no

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.