MIR1470

gene
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Also known as hsa-mir-1470

Summary

MIR1470 (microRNA 1470, HGNC:35379) is a microRNA gene on chromosome 19p13.12.

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 100302127 — 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:35379
Approved symbolMIR1470
NamemicroRNA 1470
Location19p13.12
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1470
Ensembl geneENSG00000269782
Ensembl biotypemiRNA
Entrez100302127
RNAcentralURS0000759FF8 — ncRNA, 61 nt, 5 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000600745

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000600745 — 1 exons

ExonStartEnd
ENSE000035182051544954815449608

Expression profiles

Bgee: expression breadth broad, 24 present calls, max score 76.51.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
skin of legUBERON:000151176.51gold quality
tibial arteryUBERON:000761069.62gold quality
bloodUBERON:000017869.29gold quality
Ammon’s hornUBERON:000195468.98gold quality
esophagogastric junction muscularis propriaUBERON:003584168.39gold quality
right atrium auricular regionUBERON:000663167.34gold quality
muscle layer of sigmoid colonUBERON:003580567.21gold quality
pituitary glandUBERON:000000766.47gold quality
ascending aortaUBERON:000149666.24gold quality
subcutaneous adipose tissueUBERON:000219066.02gold quality
skin of abdomenUBERON:000141665.69gold quality
esophagus mucosaUBERON:000246965.08gold quality
colonUBERON:000115564.60gold quality
omental fat padUBERON:001041463.97gold quality
lower esophagus muscularis layerUBERON:003583363.96gold quality
myometriumUBERON:000129663.31gold quality
anterior cingulate cortexUBERON:000983563.19gold quality
tibial nerveUBERON:000132362.85gold quality
right frontal lobeUBERON:000281062.01gold quality
left lobe of thyroid glandUBERON:000112061.49gold quality
amygdalaUBERON:000187661.07gold quality
spleenUBERON:000210660.20gold quality
left testisUBERON:000453340.86gold quality
right testisUBERON:000453438.29gold 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 2)

  • The present study provided the first evidences that miR-1470 mediated lapatinib induced p27 upregulation by targeting c-jun. (PMID:25545366)
  • miR-1470 regulates cell proliferation and apoptosis by targeting ALX4 in hepatocellular carcinoma. (PMID:31791584)

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.