EPM2A-DT

gene
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Summary

EPM2A-DT (EPM2A divergent transcript, HGNC:48990) is a long non-coding RNA gene on chromosome 6q24.3.

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:48990
Approved symbolEPM2A-DT
NameEPM2A divergent transcript
Location6q24.3
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000235652
Ensembl biotypelncRNA
Entrez100507557
RNAcentralURS000075F0E0 — lncRNA, 4103 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 28 — 28 lncRNA

ENST00000452617, ENST00000587426, ENST00000587540, ENST00000591489, ENST00000592775, ENST00000606388, ENST00000626833, ENST00000626919, ENST00000627375, ENST00000629681, ENST00000630041, ENST00000630919, ENST00000653352, ENST00000654828, ENST00000658327, ENST00000660586, ENST00000663890, ENST00000688715, ENST00000690526, ENST00000691670, ENST00000700853, ENST00000805026, ENST00000805027, ENST00000805028, ENST00000805029, ENST00000805030, ENST00000805031, ENST00000805032

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000452617 — 4 exons

ExonStartEnd
ENSE00001621764145881579145881648
ENSE00001685496145828361145828456
ENSE00004196894145814858145815431
ENSE00004196899145883205145885835

Expression profiles

Bgee: expression breadth ubiquitous, 217 present calls, max score 92.95.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.7811 / max 54.2742, expressed in 1465 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
703533.37841364
703490.4027202

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047392.95gold quality
colonic epitheliumUBERON:000039789.46gold quality
calcaneal tendonUBERON:000370186.61gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099184.75gold quality
adrenal tissueUBERON:001830384.02gold quality
right uterine tubeUBERON:000130283.86gold quality
right hemisphere of cerebellumUBERON:001489083.60gold quality
cerebellar hemisphereUBERON:000224583.48gold quality
cerebellar cortexUBERON:000212983.34gold quality
prefrontal cortexUBERON:000045182.97gold quality
caudate nucleusUBERON:000187381.36gold quality
nucleus accumbensUBERON:000188281.23gold quality
left ovaryUBERON:000211981.10gold quality
anterior cingulate cortexUBERON:000983580.83gold quality
right ovaryUBERON:000211880.80gold quality
cingulate cortexUBERON:000302780.77gold quality
Brodmann (1909) area 23UBERON:001355480.75gold quality
lower esophagus muscularis layerUBERON:003583380.74gold quality
cerebellumUBERON:000203780.73gold quality
lower esophagusUBERON:001347380.72gold quality
Brodmann (1909) area 9UBERON:001354080.62gold quality
middle temporal gyrusUBERON:000277180.56gold quality
dorsolateral prefrontal cortexUBERON:000983480.46gold quality
C1 segment of cervical spinal cordUBERON:000646980.34gold quality
esophagogastric junction muscularis propriaUBERON:003584180.31gold quality
primary visual cortexUBERON:000243680.27gold quality
right frontal lobeUBERON:000281080.08gold quality
neocortexUBERON:000195079.78gold quality
left lobe of thyroid glandUBERON:000112079.76gold quality
frontal cortexUBERON:000187079.65gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes5.17

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): progressive myoclonus epilepsy