MIR1260B

gene
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Also known as hsa-mir-1260b

Summary

MIR1260B (microRNA 1260b, HGNC:38258) is a microRNA gene on chromosome 11q21.

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 100422991 — 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:38258
Approved symbolMIR1260B
NamemicroRNA 1260b
Location11q21
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1260b
Ensembl geneENSG00000266192
Ensembl biotypemiRNA
OMIM615372
Entrez100422991
RNAcentralURS0000759BF7 — miRNA, 89 nt, 11 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000582890

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000582890 — 1 exons

ExonStartEnd
ENSE000027199439634143896341526

Expression profiles

Bgee: expression breadth broad, 29 present calls, max score 87.27.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548887.27gold quality
bone marrowUBERON:000237178.56gold quality
duodenumUBERON:000211476.67gold quality
right frontal lobeUBERON:000281076.29gold quality
small intestineUBERON:000210874.40gold quality
bloodUBERON:000017870.97gold quality
lungUBERON:000204867.56gold quality
multicellular organismUBERON:000046866.01gold quality
skin of abdomenUBERON:000141665.98gold quality
esophagogastric junction muscularis propriaUBERON:003584165.26gold quality
C1 segment of cervical spinal cordUBERON:000646964.64gold quality
gastrocnemiusUBERON:000138864.51gold quality
stomachUBERON:000094561.67gold quality
dorsolateral prefrontal cortexUBERON:000983461.54gold quality
heart left ventricleUBERON:000208461.49gold quality
anterior cingulate cortexUBERON:000983560.45gold quality
islet of LangerhansUBERON:000000658.87gold quality
thyroid glandUBERON:000204658.10gold quality
putamenUBERON:000187456.61gold quality
body of stomachUBERON:000116155.88gold quality
adrenal glandUBERON:000236951.66gold quality
left ovaryUBERON:000211950.24gold quality
nucleus accumbensUBERON:000188250.15gold quality
esophagus mucosaUBERON:000246949.70gold quality
testisUBERON:000047349.09gold quality
muscle layer of sigmoid colonUBERON:003580547.27gold quality
left adrenal glandUBERON:000123441.21gold quality
left adrenal gland cortexUBERON:003582537.08silver quality
left testisUBERON:000453330.45silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 12)

  • miR-1260b promoted renal cancer cell proliferation and invasion in renal cell carcinoma cells. (PMID:23591200)
  • Data suggest genistein exerts its anti-tumour effect via downregulation of miR-1260b that targeted sRRP1 and Smad4 genes in prostate cancer cells. Expression of sFRP1 and Smad4 was modulated via DNA methylation or histone modifications in PC. (PMID:24504368)
  • The miR-1260b expression in CRC was significantly higher than the expression levels in the corresponding para-carcinoma tissues (P<0.001). According to the expression levels of miR-1260b, 120 cases of CRC patients were classified into either the miR-1260b high expression group or the miR-1260b low expression group. (PMID:27399918)
  • This pilot study suggests that miR1246 and miR4644 in salivary exosomes could be candidate biomarkers for pancreatobiliary tract cancer. (PMID:27573701)
  • Regulator of G-protein signaling 22 (RGS22) was identified as a direct target of miR-1260b and was inhibited by miR-1260b. Knockdown of RGS22 increased proliferation of hepatocellular carcinoma cells. (PMID:29038925)
  • Study is the first to illustrate that miR-1260b, mediated by YY1, activates KIT signaling by targeting SOCS6 to regulate NSCLC cell proliferation and apoptosis, and is a potential biomarker and therapeutic target for NSCLC. (PMID:30737371)
  • Hypoxia-induced miR-1260b regulates vascular smooth muscle cell proliferation by targeting GDF11. (PMID:31818357)
  • Exosome-mediated transfer of miR-1260b promotes cell invasion through Wnt/beta-catenin signaling pathway in lung adenocarcinoma. (PMID:32026462)
  • Exosomal miR-1260b derived from non-small cell lung cancer promotes tumor metastasis through the inhibition of HIPK2. (PMID:34321461)
  • MiR-1260b protects against LPS-induced degenerative changes in nucleus pulposus cells through targeting TCF7L2. (PMID:35165858)
  • Promotion of tumorigenesis by miR-1260b-targeting CASP8: Potential diagnostic and prognostic marker for breast cancer. (PMID:35325509)
  • miRNA-1260b Promotes Breast Cancer Cell Migration and Invasion by Downregulating CCDC134. (PMID:36056852)

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.