MIR3173

gene
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Also known as hsa-mir-3173

Summary

MIR3173 (microRNA 3173, HGNC:38174) is a microRNA gene on chromosome 14q32.13.

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 100422981 — 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:38174
Approved symbolMIR3173
NamemicroRNA 3173
Location14q32.13
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3173
Ensembl geneENSG00000264607
Ensembl biotypemiRNA
Entrez100422981
RNAcentralURS000075C556 — miRNA, 68 nt, 4 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000580810

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000580810 — 1 exons

ExonStartEnd
ENSE000026969639513791995137986

Expression profiles

Bgee: expression breadth broad, 86 present calls, max score 85.47.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidneyUBERON:000211385.47gold quality
prefrontal cortexUBERON:000045182.76gold quality
bone marrowUBERON:000237182.03gold quality
calcaneal tendonUBERON:000370179.87gold quality
adult mammalian kidneyUBERON:000008279.70gold quality
adrenal tissueUBERON:001830377.89gold quality
bloodUBERON:000017877.68gold quality
liverUBERON:000210776.95gold quality
olfactory segment of nasal mucosaUBERON:000538676.34gold quality
monocyteCL:000057675.88gold quality
muscle of legUBERON:000138374.25gold quality
stomachUBERON:000094573.46gold quality
gastrocnemiusUBERON:000138873.15gold quality
lymph nodeUBERON:000002973.01gold quality
heartUBERON:000094872.37gold quality
islet of LangerhansUBERON:000000671.27gold quality
thoracic mammary glandUBERON:000520071.06gold quality
smooth muscle tissueUBERON:000113570.96gold quality
heart left ventricleUBERON:000208470.75gold quality
right lobe of liverUBERON:000111470.22gold quality
rectumUBERON:000105270.14gold quality
right atrium auricular regionUBERON:000663169.94gold quality
left adrenal glandUBERON:000123469.60gold quality
putamenUBERON:000187469.25gold quality
body of stomachUBERON:000116169.03gold quality
frontal cortexUBERON:000187069.01gold quality
body of pancreasUBERON:000115068.80gold quality
amygdalaUBERON:000187668.77gold quality
corpus callosumUBERON:000233668.63gold quality
intestineUBERON:000016068.15gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.92

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Generally, this study indicates that miR-3173 negatively regulates PTK2 and inhibits proliferation and invasion of B-ALL cell lines. Thus, miR-3173 may represent a potential therapeutic molecule for B-ALL intervention. (PMID:29066351)

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.