MAPT-AS1

gene
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Also known as MAPT-AS

Summary

MAPT-AS1 (MAPT antisense RNA 1, HGNC:43738) is a long non-coding RNA gene on chromosome 17q21.31.

Involved in regulatory ncRNA-mediated gene silencing. Implicated in Parkinson’s disease.

Source: NCBI Gene 100128977 — 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:43738
Approved symbolMAPT-AS1
NameMAPT antisense RNA 1
Location17q21.31
Locus typeRNA, long non-coding
StatusApproved
AliasesMAPT-AS
Ensembl geneENSG00000264589
Ensembl biotypelncRNA
Entrez100128977
RNAcentralURS000075DB76 — lncRNA, 855 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 9 lncRNA

ENST00000579244, ENST00000579599, ENST00000581125, ENST00000634876, ENST00000649665, ENST00000653949, ENST00000793286, ENST00000793287, ENST00000793288

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000579244 — 2 exons

ExonStartEnd
ENSE000026975424584365145844161
ENSE000027170584589548045895600

Expression profiles

Bgee: expression breadth ubiquitous, 108 present calls, max score 79.77.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.6217 / max 109.8355, expressed in 159 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1665580.4940143
1665590.127762

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right testisUBERON:000453479.77gold quality
left testisUBERON:000453379.45gold quality
cerebellumUBERON:000203779.31gold quality
cerebellar cortexUBERON:000212979.25gold quality
cerebellar hemisphereUBERON:000224579.25gold quality
colonic epitheliumUBERON:000039778.92gold quality
right hemisphere of cerebellumUBERON:001489078.85gold quality
testisUBERON:000047378.63gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099176.55gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047375.69gold quality
cortical plateUBERON:000534374.83gold quality
superior frontal gyrusUBERON:000266174.15gold quality
prefrontal cortexUBERON:000045172.94gold quality
temporal lobeUBERON:000187172.74gold quality
amygdalaUBERON:000187672.61gold quality
frontal cortexUBERON:000187072.24gold quality
hypothalamusUBERON:000189871.89gold quality
cerebral cortexUBERON:000095671.18gold quality
right frontal lobeUBERON:000281071.01gold quality
anterior cingulate cortexUBERON:000983570.96gold quality
brainUBERON:000095570.85gold quality
dorsolateral prefrontal cortexUBERON:000983470.51gold quality
Brodmann (1909) area 9UBERON:001354070.15gold quality
Ammon’s hornUBERON:000195469.89gold quality
putamenUBERON:000187468.66gold quality
primary visual cortexUBERON:000243668.61gold quality
cortex of kidneyUBERON:000122568.29gold quality
hindlimb stylopod muscleUBERON:000425268.23gold quality
substantia nigraUBERON:000203868.14gold quality
caudate nucleusUBERON:000187366.71gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.43

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 3)

  • MAPT-AS1 and DNMT1 have been identified as potential epigenetic regulators of MAPT expression in PD across four different brain regions. Our data also suggest that increased MAPT expression could be associated with disease state, but not with PD neuropathology severity. (PMID:27336847)
  • the level of MAPT-AS1 was correlated with the expression of MAPT, and MAPT was associated with survival time in breast cancer. (PMID:30074401)
  • MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration. (PMID:34012113)

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.