MIR4308

gene
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Also known as hsa-mir-4308

Summary

MIR4308 (microRNA 4308, HGNC:38206) is a microRNA gene on chromosome 14q22.2.

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 100422984 — 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:38206
Approved symbolMIR4308
NamemicroRNA 4308
Location14q22.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4308
Ensembl geneENSG00000265432
Ensembl biotypemiRNA
Entrez100422984
RNAcentralURS000075C52F — miRNA, 81 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000580634

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000580634 — 1 exons

ExonStartEnd
ENSE000027106165487811354878193

Expression profiles

Bgee: expression breadth broad, 49 present calls, max score 84.81.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
liverUBERON:000210784.81gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.17gold quality
adrenal tissueUBERON:001830380.72gold quality
right lobe of liverUBERON:000111477.99gold quality
bloodUBERON:000017877.31gold quality
bone marrowUBERON:000237174.85gold quality
monocyteCL:000057674.53gold quality
calcaneal tendonUBERON:000370174.28gold quality
heartUBERON:000094872.41gold quality
body of pancreasUBERON:000115072.12gold quality
adult mammalian kidneyUBERON:000008271.02gold quality
right atrium auricular regionUBERON:000663170.76gold quality
stomachUBERON:000094570.62gold quality
heart left ventricleUBERON:000208469.78gold quality
left ovaryUBERON:000211969.70gold quality
left adrenal gland cortexUBERON:003582568.82gold quality
tibial arteryUBERON:000761068.52gold quality
multicellular organismUBERON:000046867.83gold quality
left adrenal glandUBERON:000123467.52gold quality
omental fat padUBERON:001041465.98gold quality
putamenUBERON:000187465.48gold quality
esophagogastric junction muscularis propriaUBERON:003584165.33gold quality
body of stomachUBERON:000116165.19gold quality
intestineUBERON:000016065.04gold quality
nucleus accumbensUBERON:000188265.04gold quality
skin of legUBERON:000151164.89gold quality
transverse colonUBERON:000115764.11gold quality
anterior cingulate cortexUBERON:000983563.60gold quality
skin of abdomenUBERON:000141663.07gold quality
esophagus mucosaUBERON:000246962.92gold 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

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): dystonia 5