MIR4641

gene
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Also known as hsa-mir-4641

Summary

MIR4641 (microRNA 4641, HGNC:41835) is a microRNA gene on chromosome 6p21.1.

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 100616178 — 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:41835
Approved symbolMIR4641
NamemicroRNA 4641
Location6p21.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4641
Ensembl geneENSG00000266494
Ensembl biotypemiRNA
Entrez100616178
RNAcentralURS000075E7ED — miRNA, 66 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000578353

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000578353 — 1 exons

ExonStartEnd
ENSE000027022004159872341598788

Expression profiles

Bgee: expression breadth broad, 80 present calls, max score 81.82.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
lymph nodeUBERON:000002981.82gold quality
bone marrowUBERON:000237180.46gold quality
placentaUBERON:000198778.94gold quality
prefrontal cortexUBERON:000045176.57gold quality
monocyteCL:000057676.29gold quality
muscle of legUBERON:000138374.93gold quality
rectumUBERON:000105274.70gold quality
bloodUBERON:000017874.66gold quality
calcaneal tendonUBERON:000370174.29gold quality
gastrocnemiusUBERON:000138873.83gold quality
stomachUBERON:000094573.71gold quality
body of stomachUBERON:000116173.59gold quality
right lobe of liverUBERON:000111473.52gold quality
heart left ventricleUBERON:000208471.99gold quality
liverUBERON:000210771.76gold quality
islet of LangerhansUBERON:000000671.39gold quality
right adrenal gland cortexUBERON:003582771.08gold quality
right atrium auricular regionUBERON:000663171.02gold quality
body of pancreasUBERON:000115069.60gold quality
left adrenal gland cortexUBERON:003582568.68gold quality
tibial arteryUBERON:000761068.39gold quality
frontal cortexUBERON:000187068.32gold quality
ascending aortaUBERON:000149668.23gold quality
right lobe of thyroid glandUBERON:000111968.22gold quality
Ammon’s hornUBERON:000195467.84gold quality
adult mammalian kidneyUBERON:000008267.82gold quality
left coronary arteryUBERON:000162667.71gold quality
muscle layer of sigmoid colonUBERON:003580567.65gold quality
substantia nigraUBERON:000203867.57gold quality
esophagogastric junction muscularis propriaUBERON:003584167.11gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.08

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • circC3P1 acts as a tumor suppressor via enhancing PCK1 expression by sponging miR-4641 in hepatocellular carcinoma. (PMID:29608893)

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.