MIR2278

gene
On this page

Also known as hsa-mir-2278

Summary

MIR2278 (microRNA 2278, HGNC:37315) is a microRNA gene on chromosome 9q22.32.

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 100313780 — 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:37315
Approved symbolMIR2278
NamemicroRNA 2278
Location9q22.32
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-2278
Ensembl geneENSG00000252153
Ensembl biotypemiRNA
Entrez100313780
RNAcentralURS000075C899 — miRNA, 96 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000516344

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000516344 — 1 exons

ExonStartEnd
ENSE000020886219480996294810057

Expression profiles

Bgee: expression breadth broad, 73 present calls, max score 92.31.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548892.31gold quality
kidneyUBERON:000211383.42gold quality
corpus callosumUBERON:000233682.86gold quality
bloodUBERON:000017882.31gold quality
liverUBERON:000210781.54gold quality
calcaneal tendonUBERON:000370181.33gold quality
adrenal tissueUBERON:001830378.99gold quality
adult mammalian kidneyUBERON:000008278.80gold quality
stomachUBERON:000094577.78gold quality
lungUBERON:000204876.45gold quality
anterior cingulate cortexUBERON:000983573.28gold quality
endometriumUBERON:000129571.88gold quality
body of pancreasUBERON:000115071.81gold quality
monocyteCL:000057671.59gold quality
heart left ventricleUBERON:000208470.90gold quality
gastrocnemiusUBERON:000138870.77gold quality
heartUBERON:000094870.55gold quality
adrenal glandUBERON:000236970.14gold quality
substantia nigraUBERON:000203869.93gold quality
body of stomachUBERON:000116169.78gold quality
intestineUBERON:000016069.60gold quality
colonUBERON:000115569.58gold quality
muscle layer of sigmoid colonUBERON:003580568.44gold quality
right lobe of liverUBERON:000111467.69gold quality
tibial arteryUBERON:000761067.67gold quality
dorsolateral prefrontal cortexUBERON:000983467.66gold quality
ascending aortaUBERON:000149667.29gold quality
thoracic aortaUBERON:000151567.26gold quality
left adrenal glandUBERON:000123467.20gold quality
vaginaUBERON:000099667.06gold 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 1)

  • Loss of hsa-miR-2278 is associated with chronic myeloid leukemia. (PMID:25953263)

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.