MIR1265

gene
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Also known as hsa-mir-1265

Summary

MIR1265 (microRNA 1265, HGNC:35332) is a microRNA gene on chromosome 10p13.

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 100302116 — 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:35332
Approved symbolMIR1265
NamemicroRNA 1265
Location10p13
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1265
Ensembl geneENSG00000221371
Ensembl biotypemiRNA
Entrez100302116
RNAcentralURS00006A766D — miRNA, 86 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000408444

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000408444 — 1 exons

ExonStartEnd
ENSE000015650791443657614436661

Expression profiles

Bgee: expression breadth broad, 25 present calls, max score 76.84.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017876.84gold quality
endometriumUBERON:000129574.89gold quality
stomachUBERON:000094574.52gold quality
gastrocnemiusUBERON:000138873.86gold quality
body of pancreasUBERON:000115072.57gold quality
body of stomachUBERON:000116172.54gold quality
heart left ventricleUBERON:000208470.64gold quality
right atrium auricular regionUBERON:000663169.41gold quality
omental fat padUBERON:001041467.73gold quality
lower esophagus muscularis layerUBERON:003583366.53gold quality
gall bladderUBERON:000211066.15gold quality
right frontal lobeUBERON:000281065.86gold quality
rectumUBERON:000105265.76gold quality
cerebellar hemisphereUBERON:000224564.58gold quality
amygdalaUBERON:000187664.26gold quality
caudate nucleusUBERON:000187364.12gold quality
muscle layer of sigmoid colonUBERON:003580564.03gold quality
vaginaUBERON:000099663.85gold quality
skin of abdomenUBERON:000141663.81gold quality
right ovaryUBERON:000211863.29gold quality
thyroid glandUBERON:000204661.80gold quality
transverse colonUBERON:000115761.75gold quality
spleenUBERON:000210660.91gold quality
tibial nerveUBERON:000132358.47gold quality
prostate glandUBERON:000236755.68gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.49

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • miR-1265 suppresses gastric cancer progression and oncogenic autophagy by reducing CAB39 expression and regulating the AMPK-mTOR signaling pathway. (PMID:30779944)
  • CircPICALM can inhibit BC metastasis and bind to miR-1265 to block its pro-invasion activity. (PMID:31648990)

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.