MIR6077

gene
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Also known as hsa-mir-6077-1hsa-mir-6077-2

Summary

MIR6077 (microRNA 6077, HGNC:50025) is a microRNA gene on chromosome 1q21.2.

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 102466225 — 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:50025
Approved symbolMIR6077
NamemicroRNA 6077
Location1q21.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-6077-1, hsa-mir-6077-2
Ensembl geneENSG00000278596
Ensembl biotypemiRNA
Entrez102466225
RNAcentralURS000075AB26 — miRNA, 82 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000619691

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000619691 — 1 exons

ExonStartEnd
ENSE00003728199148388282148388363

Expression profiles

Bgee: expression breadth broad, 79 present calls, max score 90.26.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370190.26gold quality
bone marrowUBERON:000237179.66gold quality
bloodUBERON:000017877.28gold quality
placentaUBERON:000198777.01gold quality
monocyteCL:000057676.41gold quality
gastrocnemiusUBERON:000138874.64gold quality
adrenal tissueUBERON:001830374.51gold quality
ectocervixUBERON:001224973.26gold quality
heartUBERON:000094872.06gold quality
right coronary arteryUBERON:000162571.76gold quality
liverUBERON:000210771.60gold quality
left uterine tubeUBERON:000130371.28gold quality
adult mammalian kidneyUBERON:000008271.15gold quality
lungUBERON:000204871.06gold quality
stomachUBERON:000094570.63gold quality
right atrium auricular regionUBERON:000663170.42gold quality
right adrenal gland cortexUBERON:003582770.22gold quality
prefrontal cortexUBERON:000045170.05gold quality
heart left ventricleUBERON:000208469.59gold quality
islet of LangerhansUBERON:000000669.13gold quality
body of stomachUBERON:000116168.94gold quality
endometriumUBERON:000129568.65gold quality
fundus of stomachUBERON:000116068.61gold quality
ascending aortaUBERON:000149668.48gold quality
granulocyteCL:000009468.16gold quality
esophagogastric junction muscularis propriaUBERON:003584167.96gold quality
lower esophagus muscularis layerUBERON:003583367.84gold quality
amygdalaUBERON:000187667.33gold quality
frontal cortexUBERON:000187067.17gold quality
right lobe of liverUBERON:000111466.95gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.57

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • MicroRNA-6077 enhances the sensitivity of patients-derived lung adenocarcinoma cells to anlotinib by repressing the activation of glucose transporter 1 pathway. (PMID:31421224)

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.