MIR6815

gene
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Also known as hsa-mir-6815

Summary

MIR6815 (microRNA 6815, HGNC:50225) is a microRNA gene on chromosome 21q22.3.

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 102465489 — 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:50225
Approved symbolMIR6815
NamemicroRNA 6815
Location21q22.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6815
Ensembl geneENSG00000275167
Ensembl biotypemiRNA
Entrez102465489
RNAcentralURS000075C175 — miRNA, 61 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000611994

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000611994 — 1 exons

ExonStartEnd
ENSE000037179014547826645478326

Expression profiles

Bgee: expression breadth broad, 77 present calls, max score 83.49.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548883.49gold quality
bloodUBERON:000017876.51gold quality
body of stomachUBERON:000116174.95gold quality
liverUBERON:000210774.49gold quality
fundus of stomachUBERON:000116074.38gold quality
monocyteCL:000057674.37gold quality
gastrocnemiusUBERON:000138873.37gold quality
stomachUBERON:000094572.96gold quality
endocervixUBERON:000045872.92gold quality
tibial arteryUBERON:000761072.59gold quality
popliteal arteryUBERON:000225072.56gold quality
heart left ventricleUBERON:000208472.33gold quality
prefrontal cortexUBERON:000045172.18gold quality
right lobe of liverUBERON:000111472.18gold quality
body of pancreasUBERON:000115071.81gold quality
calcaneal tendonUBERON:000370171.42gold quality
left coronary arteryUBERON:000162671.38gold quality
urinary bladderUBERON:000125570.35gold quality
ectocervixUBERON:001224969.47gold quality
heartUBERON:000094869.29gold quality
endometriumUBERON:000129569.18gold quality
ascending aortaUBERON:000149668.79gold quality
thoracic aortaUBERON:000151568.72gold quality
lower esophagus muscularis layerUBERON:003583368.66gold quality
left adrenal gland cortexUBERON:003582568.63gold quality
thoracic mammary glandUBERON:000520067.90gold quality
multicellular organismUBERON:000046867.81gold quality
transverse colonUBERON:000115767.55gold quality
Ammon’s hornUBERON:000195467.47gold quality
lungUBERON:000204867.46gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.21

Regulation

Is transcription factor: no

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.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): Knobloch syndrome 1