MIR4310

gene
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Also known as hsa-mir-4310

Summary

MIR4310 (microRNA 4310, HGNC:38383) is a microRNA gene on chromosome 15q15.1.

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 100423013 — 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:38383
Approved symbolMIR4310
NamemicroRNA 4310
Location15q15.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4310
Ensembl geneENSG00000264850
Ensembl biotypemiRNA
Entrez100423013
RNAcentralURS00007599FC — ncRNA, 57 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000582950

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000582950 — 1 exons

ExonStartEnd
ENSE000027119374186649541866551

Expression profiles

Bgee: expression breadth broad, 26 present calls, max score 97.34.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548897.34gold quality
Ammon’s hornUBERON:000195473.94gold quality
bloodUBERON:000017872.70gold quality
fundus of stomachUBERON:000116071.16gold quality
body of stomachUBERON:000116169.85gold quality
amygdalaUBERON:000187669.48gold quality
anterior cingulate cortexUBERON:000983568.15gold quality
tibial arteryUBERON:000761067.68gold quality
skin of abdomenUBERON:000141667.62gold quality
omental fat padUBERON:001041466.93gold quality
urinary bladderUBERON:000125566.60gold quality
skin of legUBERON:000151166.18gold quality
right frontal lobeUBERON:000281066.13gold quality
tibial nerveUBERON:000132366.09gold quality
esophagus mucosaUBERON:000246965.47gold quality
cerebellar hemisphereUBERON:000224565.32gold quality
thyroid glandUBERON:000204665.09gold quality
vaginaUBERON:000099665.02gold quality
prostate glandUBERON:000236763.42gold quality
right hemisphere of cerebellumUBERON:001489063.41gold quality
subcutaneous adipose tissueUBERON:000219062.65gold quality
esophagogastric junction muscularis propriaUBERON:003584162.49gold quality
endometriumUBERON:000129560.24gold quality
testisUBERON:000047348.49gold quality
left testisUBERON:000453348.27gold quality
right testisUBERON:000453441.88gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.16

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • knockdown of CASC15 significantly inhibited the proliferation, migration and invasion of colon cancer cells in vitro and in vivo. Following mechanistic experiments, CASC15 was observed to act as a sponge to suppress microRNA (miR)4310 that targeted LGR5. (PMID:29956772)
  • Differentially expressed miR-4310 functions as a tumor suppressor in colorectal cancer. (PMID:37545284)

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.