MIR1202

gene
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Also known as hsa-mir-1202

Summary

MIR1202 (microRNA 1202, HGNC:35268) is a microRNA gene on chromosome 6q25.3.

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 100302259 — 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:35268
Approved symbolMIR1202
NamemicroRNA 1202
Location6q25.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1202
Ensembl geneENSG00000221456
Ensembl biotypemiRNA
Entrez100302259
RNAcentralURS000075E4E5 — miRNA, 83 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000408529

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000408529 — 1 exons

ExonStartEnd
ENSE00001565164155946797155946879

Expression profiles

Bgee: expression breadth broad, 31 present calls, max score 80.90.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017880.90gold quality
monocyteCL:000057673.34gold quality
calcaneal tendonUBERON:000370171.93gold quality
heartUBERON:000094871.53gold quality
gastrocnemiusUBERON:000138870.22gold quality
Ammon’s hornUBERON:000195467.16gold quality
tibial arteryUBERON:000761066.63gold quality
body of uterusUBERON:000985364.84gold quality
amygdalaUBERON:000187664.75gold quality
ascending aortaUBERON:000149664.66gold quality
subcutaneous adipose tissueUBERON:000219064.25gold quality
esophagus mucosaUBERON:000246964.02gold quality
lower esophagus muscularis layerUBERON:003583363.87gold quality
omental fat padUBERON:001041463.64gold quality
body of stomachUBERON:000116162.95gold quality
skin of legUBERON:000151162.54gold quality
esophagogastric junction muscularis propriaUBERON:003584162.24gold quality
minor salivary glandUBERON:000183061.53gold quality
skin of abdomenUBERON:000141660.98gold quality
vaginaUBERON:000099659.58gold quality
thyroid glandUBERON:000204659.25gold quality
right lobe of thyroid glandUBERON:000111959.02gold quality
left lobe of thyroid glandUBERON:000112058.96gold quality
tibial nerveUBERON:000132358.56gold quality
upper lobe of left lungUBERON:000895257.56gold quality
spleenUBERON:000210657.14gold quality
pituitary glandUBERON:000000756.69gold quality
thoracic mammary glandUBERON:000520056.16gold quality
corpus callosumUBERON:000233653.96gold quality
colonUBERON:000115547.49gold 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 14)

  • results suggest that miR-1202 is associated with the pathophysiology of depression and is a potential target for new antidepressant treatments (PMID:24908571)
  • Evidence show that miR-1202 exists in a dose-dependent relationship with expression of the gene GRM4 in the human prefrontal cortex and its expression is related to successful antidepressant treatment. (PMID:25315250)
  • We found that either miR-1202 silencing or miR-196a overexpression affected AN3CA and HEC-1-A cells by increasing their apoptosis level and inducing G1 phase arrest while decreasing their migratory and invasive abilities. Inhibitors of miR-1202 and miR196a may exert a protective effect, suggesting that miR-1202 and miR196a may serve as biomarkers for evaluating the effectiveness of endometrial cancer treatment (PMID:28440476)
  • our data indicate that miR-1202 suppresses proliferation and induces endoplasmic reticulum stress and apoptosis through targeting and inhibiting Rab1A in glioma cells. These results suggest miR-1202 as a potential therapeutic target for the treatment of glioma patients. (PMID:28443461)
  • CDK14 mediated miR-1202 to exert its anti-tumor effects. (PMID:29217161)
  • Changes in expression of lncRNA-GAS5, miRNA-661, miRNA-1202 and MMP9 in M2 macrophages are involved in varicose disease. (PMID:30558403)
  • MiR-1202 Exerts Neuroprotective Effects on OGD/R Induced Inflammation in HM Cell by Negatively Regulating Rab1a Involved in TLR4/NF-kappaB Signaling Pathway. (PMID:32124161)
  • MicroRNA-1202 plays a vital role in osteoarthritis via KCNQ1OT1 has-miR-1202-ETS1 regulatory pathway. (PMID:32252801)
  • MiRNA-1202 promotes the TGF-beta1-induced proliferation, differentiation and collagen production of cardiac fibroblasts by targeting nNOS. (PMID:34428251)
  • IGF2BP3 Worsens Lung Cancer through Modifying Long Non-coding RNA CERS6-AS1/microRNA-1202 Axis. (PMID:35702784)
  • Involvement of FAM170B-AS1, hsa-miR-1202, and hsa-miR-146a-5p in breast cancer. (PMID:38250762)
  • miR-1202 acts as anti-oncomiR in myeloid leukaemia by down-modulating GATA-1S expression. (PMID:38350611)
  • miR-1202 regulates BPH-1 cell proliferation, apoptosis, and epithelial-to-mesenchymal transition through targeting HMGCL. (PMID:38551020)
  • Exosomal miR-1202 mediates Brodmann Area 44 functional connectivity changes in medication-free patients with major depressive disorder: An fMRI study. (PMID:38608766)

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.