MIR1290

gene
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Also known as hsa-mir-1290

Summary

MIR1290 (microRNA 1290, HGNC:35283) is a microRNA gene on chromosome 1p36.13.

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 100302276 — 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:35283
Approved symbolMIR1290
NamemicroRNA 1290
Location1p36.13
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1290
Ensembl geneENSG00000221662
Ensembl biotypemiRNA
Entrez100302276
RNAcentralURS000075D458 — miRNA, 78 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000408735

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000408735 — 1 exons

ExonStartEnd
ENSE000015653701889707118897148

Expression profiles

Bgee: expression breadth broad, 91 present calls, max score 84.74.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830384.74gold quality
bone marrowUBERON:000237181.11gold quality
endometriumUBERON:000129580.47gold quality
calcaneal tendonUBERON:000370179.23gold quality
right uterine tubeUBERON:000130278.73gold quality
monocyteCL:000057677.92gold quality
kidneyUBERON:000211375.57gold quality
muscle of legUBERON:000138374.51gold quality
bloodUBERON:000017874.44gold quality
placentaUBERON:000198774.43gold quality
liverUBERON:000210773.64gold quality
gastrocnemiusUBERON:000138873.34gold quality
granulocyteCL:000009472.62gold quality
mucosa of stomachUBERON:000119972.24gold quality
adult mammalian kidneyUBERON:000008272.20gold quality
islet of LangerhansUBERON:000000671.28gold quality
stomachUBERON:000094570.96gold quality
olfactory segment of nasal mucosaUBERON:000538670.84gold quality
smooth muscle tissueUBERON:000113570.78gold quality
right lobe of liverUBERON:000111470.73gold quality
heartUBERON:000094869.94gold quality
right atrium auricular regionUBERON:000663169.24gold quality
body of pancreasUBERON:000115068.71gold quality
lungUBERON:000204868.44gold quality
tibial arteryUBERON:000761068.38gold quality
right ovaryUBERON:000211868.14gold quality
heart left ventricleUBERON:000208467.88gold quality
Ammon’s hornUBERON:000195467.82gold quality
rectumUBERON:000105267.72gold quality
body of stomachUBERON:000116167.51gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.66

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 40)

  • miRNA-584 and miRNA-1290, upregulated by the CagA protein of H, pylori, interfere with cell differentiation and are implicated in metaplasia and tissue remodeling. (PMID:22536353)
  • up-regulation of miR-1290 in colon cancer cells impaired cytokinesis and affected reprogramming. (PMID:23142292)
  • Downregulation of miR-1290 is associated with estrogen receptor alpha-positive breast cancer. (PMID:23183268)
  • The detection of elevated circulating miR-1290 has the potential to improve the early detection of pancreatic cancer. (PMID:23697990)
  • Knockdown of miR-1290 inhibited differentiation and induced proliferation in differentiated neurons. (PMID:24407235)
  • A signature comprising three miRNAs (miR1290, miR196b, and miR135a*) enabled the prediction of a chemotherapeutic response (rather than progression-free and overall survival) with high accuracy in patients with recurring lung adenocarcinoma (PMID:25142144)
  • We report that miR-1290 directly targets the NAT1 3’-UTR and that NAT1 protein expression is correlated with improved OS of breast cancer patients. (PMID:25528056)
  • antagomir-1290 significantly inhibited the proliferation, clonogenicity, invasion, and migration of CD133(+) cells by targeting fyn-related Src family tyrosine kinase. (PMID:25783528)
  • Suggest that miR-1290 may play an oncogenic role in cellular processes of esophageal squamous cell carcinoma. (PMID:25805931)
  • MiR-196b and miR-1290 targeted the 3’ untranslated region of HIV-1 and affected its expression. (PMID:26469550)
  • Data suggest miR-1290 as the new oncomiR involved in laryngeal squamous cell carcinoma pathogenesis probably through downregulation of its target genes MAF and ITPR2. (PMID:26694163)
  • Anti-miR-1246 and anti-miR-1290 suppressed proliferation, sphere-formation, colony formation and invasion of NSCLC. CSCs-associated miR-1246, or miR-1290 may be important in the invasion or metastasis of NSCLC. (PMID:26711929)
  • Tumor-initiating cell-specific miR-1246 and miR-1290 expression converge to promote non-small cell lung cancer progression. (PMID:27325363)
  • Serum miR-1290 is a novel biomarker for early detection, recurrence, and prognosis in colorectal cancer (CRC). (PMID:27502702)
  • AA can protect cardiomyocytes against hypoxia-induced apoptosis through regulating the miR-1290/HIF3A/HIF-1alpha axis, and miR-1290 may be a potential target in the prevention of myocardial ischemia-reperfusion injury (PMID:28686797)
  • Compared to noncancerous esophageal mucosa, miR-1290 expression was upregulated, while NFIX mRNA expression was downregulated in ESCC tissues. Data suggest that the dysregulation of miR-1290-NFIX axis may play crucial roles in esophageal carcinogenesis and progression. (PMID:28800311)
  • Luciferase reporter assay revealed that miR-1290 directly bound to the 3’-UTR of INPP4B; the mutated seed sites in miR-1290 abrogated this effect. Double knockdown of INPP4B and miR-1290 promoted CRC cell proliferation, suggesting miR-1290 promoted CRC cell proliferation by targeting INPP4B. (PMID:28915933)
  • The orthotopic implantation model showed that miR-1290 overexpression promoted tumor growth while LHX6 overexpression inhibited it. MiR-1290 could promote glioma cell propagation and metastasis by inhibiting LHX6. (PMID:29226322)
  • Data suggest that MIR1290 expression is remarkably upregulated in non-small-cell lung carcinoma tissues compared to adjacent normal lung tissues; IRF2 appears to be a direct target of MIR1290. (MIR1290 = microRNA-1290; IRF2 = interferon regulatory factor-2) (PMID:29275213)
  • quantification of miR-1290 as a circulating biomarker for pancreatic cancer (PMID:30401891)
  • Overexpression of miR-1290 could suppress IKK1 in pancreatic ductal adenocarcinoma, suggesting that miR-1290 partially controls cell proliferation, invasion, and migration by inhibiting the expression of IKK1 via the p62/ NRF2/MDM2 pathway. (PMID:30463064)
  • Plasma miR-1290 is a novel and specific biomarker that can effectively differentiate necrotizing enterocolitis (NEC) cases from neonatal sepsis. (PMID:30529132)
  • The results suggest that exosomal miR-1290 enhances gastric cancer cell proliferation and invasion by targeting NKD1 (naked cuticle homolog 1) mRNA and downregulating NKD1 expression. (PMID:31435644)
  • Neurons can upregulate Cav-1 to increase intake of endothelial cells-derived extracellular vesicles that attenuate apoptosis via miR-1290. (PMID:31740664)
  • MiR-1290 targets CCNG2 to promote the metastasis of oral squamous cell carcinoma. (PMID:31841213)
  • Hsa_circ_0056558 regulates cyclin-dependent kinase 6 by sponging microRNA-1290 to suppress the proliferation and differentiation in ankylosing spondylitis. (PMID:33685301)
  • MiR-1290 promotes myoblast differentiation and protects against myotube atrophy via Akt/p70/FoxO3 pathway regulation. (PMID:33722298)
  • LncRNA-NONHSAT024778 promote the proliferation and invasion of chordoma cell by regulating miR-1290/Robo1 axis. (PMID:33767589)
  • Detection significance of miR-3662, miR-146a, and miR-1290 in serum exosomes of breast cancer patients. (PMID:34269309)
  • Loss of the MAF Transcription Factor in Laryngeal Squamous Cell Carcinoma. (PMID:34356658)
  • Circulating MiR-1290 as a potential diagnostic and disease monitoring biomarker of human gastrointestinal tumors. (PMID:34479528)
  • miR-1290 promotes IL-8-mediated vascular endothelial cell adhesion by targeting GSK-3beta. (PMID:34837150)
  • The potential role of miR-1290 in cancer progression, diagnosis, prognosis, and treatment: An oncomiR or onco-suppressor microRNA? (PMID:34897783)
  • Tissue miR-200c-3p and circulating miR-1290 as potential prognostic biomarkers for colorectal cancer. (PMID:35145164)
  • [Effect of miR1290 on the growth of endometrial cancer and the related mechanism]. (PMID:35184456)
  • Hsa-miR-1290 is associated with stemness and invasiveness in prostate cancer cell lines by targeting RORA. (PMID:35220610)
  • Polymorphism in the human arylamine N-acetyltransferase 1 gene 3’-untranslated region determines polyadenylation signal usage. (PMID:35358480)
  • Identification of a novel circ_0001946/miR-1290/SOX6 ceRNA network in esophageal squamous cell cancer. (PMID:35411716)
  • miR-1290 modulates the radioresistance of triple-negative breast cancer by targeting NLRP3-mediated pyroptosis. (PMID:35471684)
  • Circular_0086414 induces SPARC like 1 (SPARCL1) production to inhibit esophageal cancer cell proliferation, invasion and glycolysis and induce cell apoptosis by sponging miR-1290. (PMID:35549806)

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.