MIR194-2HG

gene
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Summary

MIR194-2HG (MIR194-2 host gene, HGNC:51946) is a long non-coding RNA gene on chromosome 11q13.1.

Predicted to be involved in miRNA-mediated post-transcriptional gene silencing. Predicted to be part of RISC complex.

Source: NCBI Gene 105369343 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (lncRNA) — 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:51946
Approved symbolMIR194-2HG
NameMIR194-2 host gene
Location11q13.1
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000229719
Ensembl biotypelncRNA
Entrez105369343
RNAcentralURS00008E3A09 — lncRNA, 2521 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 6 lncRNA

ENST00000413053, ENST00000687544, ENST00000710929, ENST00000710930, ENST00000719982, ENST00000719983

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000413053 — 2 exons

ExonStartEnd
ENSE000016085746489341164893449
ENSE000040141226488956064893167

Expression profiles

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

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.7668 / max 209.0251, expressed in 59 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1205080.766859

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
mucosa of transverse colonUBERON:000499190.26gold quality
transverse colonUBERON:000115783.34gold quality
small intestine Peyer’s patchUBERON:000345480.51gold quality
rectumUBERON:000105278.85gold quality
small intestineUBERON:000210878.34gold quality
colonic epitheliumUBERON:000039775.45gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047372.88silver quality
intestineUBERON:000016070.55gold quality
colonUBERON:000115568.37gold quality
bone marrow cellCL:000209268.21silver quality
body of stomachUBERON:000116167.49gold quality
large intestineUBERON:000005967.34gold quality
right lobe of liverUBERON:000111467.15gold quality
gingival epitheliumUBERON:000194966.88gold quality
superficial temporal arteryUBERON:000161465.92gold quality
stomachUBERON:000094564.55gold quality
mucosa of stomachUBERON:000119963.90gold quality
duodenumUBERON:000211462.70gold quality
vermiform appendixUBERON:000115461.95gold quality
mucosa of paranasal sinusUBERON:000503061.19gold quality
gall bladderUBERON:000211060.55gold quality
gingivaUBERON:000182859.66gold quality
hindlimb stylopod muscleUBERON:000425259.16gold quality
germinal epithelium of ovaryUBERON:000130459.04gold quality
body of pancreasUBERON:000115058.17gold quality
liverUBERON:000210757.48gold quality
caecumUBERON:000115357.20gold quality
pancreasUBERON:000126455.85gold quality
tonsilUBERON:000237255.65gold quality
muscle layer of sigmoid colonUBERON:003580555.34gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes12.57

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 5)

  • miR-194 regulated the progression of hepatocellular carcinoma through directly inhibiting the expression of MAP4K4 (PMID:26722431)
  • These findings suggested that miR-194 inhibits proliferation and metastasis and reverses cisplatin-resistance of non-small cell lung cancer cells (PMID:26909612)
  • The present study…identified miR-194 as predictive biomarker of response to preoperative chemoradiotherapy for locally advanced rectal cancer (PMID:28870889)
  • Downregulation of serum miR-194 predicts poor prognosis in osteosarcoma patients. (PMID:32172218)
  • miR-194-5p inhibits SLC40A1 expression to induce cisplatin resistance in ovarian cancer. (PMID:32534701)

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.