MIR649

gene
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Also known as hsa-mir-649

Summary

MIR649 (microRNA 649, HGNC:32905) is a microRNA gene on chromosome 22q11.21.

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 693234 — 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:32905
Approved symbolMIR649
NamemicroRNA 649
Location22q11.21
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-649
Ensembl geneENSG00000207575
Ensembl biotypemiRNA
Entrez693234
RNAcentralURS00006DE1AC — miRNA, 97 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000384843

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000384843 — 1 exons

ExonStartEnd
ENSE000014998502103417621034272

Expression profiles

Bgee: expression breadth broad, 51 present calls, max score 88.97.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
skeletal muscle tissueUBERON:000113488.97gold quality
muscle of legUBERON:000138376.98gold quality
gastrocnemiusUBERON:000138876.82gold quality
bloodUBERON:000017875.90gold quality
body of stomachUBERON:000116174.01gold quality
placentaUBERON:000198772.74gold quality
right atrium auricular regionUBERON:000663171.97gold quality
islet of LangerhansUBERON:000000671.86gold quality
substantia nigraUBERON:000203871.72gold quality
muscle layer of sigmoid colonUBERON:003580571.00gold quality
heart left ventricleUBERON:000208470.02gold quality
ovaryUBERON:000099269.19gold quality
colonUBERON:000115568.53gold quality
body of uterusUBERON:000985368.48gold quality
transverse colonUBERON:000115767.99gold quality
omental fat padUBERON:001041467.92gold quality
left ovaryUBERON:000211967.18gold quality
vaginaUBERON:000099667.06gold quality
esophagus mucosaUBERON:000246966.97gold quality
right adrenal glandUBERON:000123366.86gold quality
left adrenal glandUBERON:000123466.84gold quality
amygdalaUBERON:000187666.68gold quality
esophagogastric junction muscularis propriaUBERON:003584166.55gold quality
subcutaneous adipose tissueUBERON:000219066.39gold quality
tibial nerveUBERON:000132365.71gold quality
Ammon’s hornUBERON:000195465.67gold quality
right adrenal gland cortexUBERON:003582765.42gold quality
nucleus accumbensUBERON:000188265.05gold quality
ascending aortaUBERON:000149664.39gold quality
cerebellar hemisphereUBERON:000224563.71gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.65

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Taken together, this present study indicates that miR-649 promotes herpes simplex virus type 1 replication through regulation of the MALT1-mediated antiviral signaling pathway and suggests a promising target for antiviral therapies. (PMID:27813118)

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.