MIR6891

gene
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Also known as hsa-mir-6891

Summary

MIR6891 (microRNA 6891, HGNC:50243) is a microRNA gene on chromosome 6p21.33.

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 102465537 — 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:50243
Approved symbolMIR6891
NamemicroRNA 6891
Location6p21.33
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6891
Ensembl geneENSG00000277402
Ensembl biotypemiRNA
Entrez102465537
RNAcentralURS000075E69A — miRNA, 93 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000618788

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000618788 — 1 exons

ExonStartEnd
ENSE000037336823135522431355316

Expression profiles

Bgee: expression breadth ubiquitous, 111 present calls, max score 97.74.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
granulocyteCL:000009497.74gold quality
bone marrowUBERON:000237197.09gold quality
monocyteCL:000057693.30gold quality
apex of heartUBERON:000209891.00gold quality
bloodUBERON:000017890.85gold quality
vermiform appendixUBERON:000115490.49gold quality
lower esophagus mucosaUBERON:003583487.97gold quality
spleenUBERON:000210687.01gold quality
olfactory segment of nasal mucosaUBERON:000538687.00gold quality
sural nerveUBERON:001548886.19gold quality
skeletal muscle tissueUBERON:000113485.74gold quality
mucosa of transverse colonUBERON:000499185.43gold quality
upper lobe of left lungUBERON:000895283.40gold quality
left uterine tubeUBERON:000130382.84gold quality
small intestineUBERON:000210882.83gold quality
small intestine Peyer’s patchUBERON:000345482.37gold quality
skin of abdomenUBERON:000141682.14gold quality
lungUBERON:000204881.56gold quality
duodenumUBERON:000211481.51gold quality
zone of skinUBERON:000001481.40gold quality
kidneyUBERON:000211381.36gold quality
adult mammalian kidneyUBERON:000008281.28gold quality
islet of LangerhansUBERON:000000681.20gold quality
skin of legUBERON:000151180.81gold quality
omental fat padUBERON:001041480.30gold quality
adipose tissueUBERON:000101380.03gold quality
subcutaneous adipose tissueUBERON:000219079.82gold quality
myometriumUBERON:000129679.68gold quality
transverse colonUBERON:000115779.16gold quality
intestineUBERON:000016079.11gold 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)

  • X-linked genes exhibit miR6891-5p-regulated skewing in Sjogren’s syndrome. (PMID:35538149)
  • Exosomes from Intrahepatic Cholestasis of Pregnancy Induce Cell Apoptosis Through the miRNA-6891-5p/YWHAE Pathway. (PMID:38361148)

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.