ANKRD34C-AS1

gene
On this page

Summary

ANKRD34C-AS1 (ANKRD34C antisense RNA 1, HGNC:48618) is a long non-coding RNA gene on chromosome 15q25.1.

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:48618
Approved symbolANKRD34C-AS1
NameANKRD34C antisense RNA 1
Location15q25.1
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000259234
Ensembl biotypelncRNA
Entrez729911
RNAcentralURS000075B35A — lncRNA, 693 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 32 — 32 lncRNA

ENST00000557790, ENST00000558297, ENST00000559225, ENST00000559979, ENST00000560452, ENST00000560533, ENST00000560732, ENST00000560872, ENST00000661423, ENST00000661500, ENST00000668181, ENST00000671603, ENST00000685737, ENST00000686264, ENST00000689461, ENST00000689752, ENST00000692103, ENST00000692216, ENST00000692425, ENST00000701040, ENST00000701559, ENST00000773170, ENST00000773171, ENST00000773172, ENST00000773173, ENST00000773174, ENST00000773175, ENST00000773176, ENST00000773177, ENST00000773178, ENST00000773179, ENST00000773180

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000557790 — 4 exons

ExonStartEnd
ENSE000025428097926070579260846
ENSE000025514157926022979260301
ENSE000025579517923530179236928
ENSE000041379057928364979283945

Expression profiles

Bgee: expression breadth ubiquitous, 104 present calls, max score 77.78.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.5703 / max 34.9190, expressed in 90 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1511770.307484
1511780.262981

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
superior frontal gyrusUBERON:000266177.78gold quality
prefrontal cortexUBERON:000045176.38gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047374.83silver quality
frontal cortexUBERON:000187074.80gold quality
islet of LangerhansUBERON:000000673.09gold quality
primary visual cortexUBERON:000243673.07gold quality
nucleus accumbensUBERON:000188272.15gold quality
right frontal lobeUBERON:000281072.13gold quality
dorsolateral prefrontal cortexUBERON:000983472.12gold quality
Brodmann (1909) area 9UBERON:001354072.05gold quality
cerebral cortexUBERON:000095671.90gold quality
anterior cingulate cortexUBERON:000983570.22gold quality
hypothalamusUBERON:000189869.38gold quality
brainUBERON:000095569.12gold quality
testisUBERON:000047368.78gold quality
right hemisphere of cerebellumUBERON:001489068.67gold quality
cerebellumUBERON:000203768.63gold quality
cerebellar cortexUBERON:000212968.59gold quality
cerebellar hemisphereUBERON:000224568.50gold quality
pituitary glandUBERON:000000768.46gold quality
caudate nucleusUBERON:000187365.83gold quality
Ammon’s hornUBERON:000195465.58gold quality
adenohypophysisUBERON:000219665.39gold quality
putamenUBERON:000187465.16gold quality
temporal lobeUBERON:000187163.77gold quality
amygdalaUBERON:000187663.59gold quality
ventricular zoneUBERON:000305361.77gold quality
ganglionic eminenceUBERON:000402361.27gold quality
cortical plateUBERON:000534360.54gold quality
pancreasUBERON:000126459.38gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.95

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): EDICT syndrome