HPN-AS1

gene
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Summary

HPN-AS1 (HPN antisense RNA 1, HGNC:47041) is a long non-coding RNA gene on chromosome 19q13.11-q13.12.

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:47041
Approved symbolHPN-AS1
NameHPN antisense RNA 1
Location19q13.11-q13.12
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000227392
Ensembl biotypelncRNA
Entrez100128675
RNAcentralURS000075C3F8 — lncRNA, 3681 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 32 — 32 lncRNA

ENST00000392227, ENST00000653822, ENST00000666194, ENST00000668923, ENST00000702186, ENST00000796454, ENST00000796455, ENST00000796456, ENST00000796457, ENST00000796458, ENST00000796459, ENST00000796460, ENST00000796461, ENST00000796462, ENST00000796463, ENST00000796464, ENST00000796465, ENST00000796466, ENST00000796467, ENST00000796468, ENST00000796469, ENST00000796470, ENST00000796471, ENST00000796472, ENST00000796473, ENST00000796474, ENST00000796475, ENST00000796476, ENST00000796477, ENST00000796478, ENST00000796479, ENST00000796480

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000392227 — 4 exons

ExonStartEnd
ENSE000016408123505905935059778
ENSE000017176273508695635087100
ENSE000017344323510622935106304
ENSE000018002523509920535099387

Expression profiles

Bgee: expression breadth ubiquitous, 117 present calls, max score 85.26.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.8437 / max 104.7166, expressed in 68 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1804790.516265
1804800.265460
1804810.062238

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right lobe of liverUBERON:000111485.26gold quality
liverUBERON:000210785.20gold quality
body of pancreasUBERON:000115079.39gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047378.03silver quality
cortex of kidneyUBERON:000122575.07gold quality
metanephros cortexUBERON:001053375.02gold quality
substantia nigraUBERON:000203873.87gold quality
C1 segment of cervical spinal cordUBERON:000646973.26gold quality
Ammon’s hornUBERON:000195472.31gold quality
kidneyUBERON:000211371.70gold quality
pancreasUBERON:000126471.59gold quality
adult mammalian kidneyUBERON:000008270.81gold quality
corpus callosumUBERON:000233670.16gold quality
primary visual cortexUBERON:000243669.83gold quality
putamenUBERON:000187468.24gold quality
Brodmann (1909) area 9UBERON:001354067.76gold quality
temporal lobeUBERON:000187167.74gold quality
amygdalaUBERON:000187667.67gold quality
gastrocnemiusUBERON:000138866.34gold quality
prefrontal cortexUBERON:000045165.77gold quality
muscle of legUBERON:000138365.56gold quality
hindlimb stylopod muscleUBERON:000425265.21gold quality
body of stomachUBERON:000116164.89gold quality
skeletal muscle tissueUBERON:000113464.64gold quality
cerebral cortexUBERON:000095664.61gold quality
frontal cortexUBERON:000187064.41gold quality
hypothalamusUBERON:000189863.97gold quality
muscle tissueUBERON:000238563.76gold quality
dorsolateral prefrontal cortexUBERON:000983463.48gold quality
stomachUBERON:000094563.44gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.13

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): irritable bowel syndrome