MIR4300

gene
On this page

Also known as hsa-mir-4300

Summary

MIR4300 (microRNA 4300, HGNC:38184) is a microRNA gene on chromosome 11q14.1.

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 100422823 — 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:38184
Approved symbolMIR4300
NamemicroRNA 4300
Location11q14.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4300
Ensembl geneENSG00000264110
Ensembl biotypemiRNA
Entrez100422823
RNAcentralURS000075C0A4 — miRNA, 96 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000581016

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000581016 — 1 exons

ExonStartEnd
ENSE000027275698189074181890836

Expression profiles

Bgee: expression breadth broad, 22 present calls, max score 86.20.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
intestineUBERON:000016086.20gold quality
monocyteCL:000057677.94gold quality
right hemisphere of cerebellumUBERON:001489070.61gold quality
Ammon’s hornUBERON:000195470.21gold quality
lungUBERON:000204870.12gold quality
skin of legUBERON:000151168.74gold quality
body of stomachUBERON:000116168.57gold quality
Brodmann (1909) area 9UBERON:001354067.86gold quality
cerebellar hemisphereUBERON:000224567.61gold quality
amygdalaUBERON:000187666.40gold quality
caudate nucleusUBERON:000187366.38gold quality
dorsolateral prefrontal cortexUBERON:000983466.36gold quality
esophagogastric junction muscularis propriaUBERON:003584166.18gold quality
left lobe of thyroid glandUBERON:000112065.94gold quality
substantia nigraUBERON:000203865.61gold quality
upper lobe of left lungUBERON:000895264.54gold quality
skin of abdomenUBERON:000141663.61gold quality
prostate glandUBERON:000236762.14gold quality
corpus callosumUBERON:000233656.16gold quality
right frontal lobeUBERON:000281051.03gold quality
right testisUBERON:000453446.32gold quality
left testisUBERON:000453345.28gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.99

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • In silico and in vitro analyses identified a functional variant, rs35333564 in MIR4300HG, the host gene of a microRNA, MIR4300. The genomic region containing rs35333564 had enhancer activity, which was decreased in its risk allele. Data suggest that decrease of MIR4300 is related to AIS progression. (PMID:29016859)

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.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): adolescent idiopathic scoliosis