SYNE1-AS1
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Summary
SYNE1-AS1 (SYNE1 antisense RNA 1, HGNC:40793) is a long non-coding RNA gene on chromosome 6q25.2.
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:40793 |
| Approved symbol | SYNE1-AS1 |
| Name | SYNE1 antisense RNA 1 |
| Location | 6q25.2 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000234577 |
| Ensembl biotype | lncRNA |
| Entrez | 100505475 |
| RNAcentral | URS000075D5DF — lncRNA, 718 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 lncRNA
ENST00000412161
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000412161 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00004142692 | 152381060 | 152381777 |
| ENSE00004142693 | 152380489 | 152380593 |
Expression profiles
Bgee: expression breadth ubiquitous, 113 present calls, max score 71.07.
Top tissues by expression
113 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| bone marrow cell | CL:0002092 | 71.07 | silver quality |
| skeletal muscle tissue | UBERON:0001134 | 69.42 | gold quality |
| ganglionic eminence | UBERON:0004023 | 66.77 | gold quality |
| ventricular zone | UBERON:0003053 | 66.50 | gold quality |
| bone marrow | UBERON:0002371 | 64.66 | silver quality |
| hindlimb stylopod muscle | UBERON:0004252 | 61.90 | gold quality |
| gall bladder | UBERON:0002110 | 61.09 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 60.24 | gold quality |
| heart left ventricle | UBERON:0002084 | 59.98 | gold quality |
| islet of Langerhans | UBERON:0000006 | 59.58 | gold quality |
| heart | UBERON:0000948 | 58.94 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 57.98 | gold quality |
| prefrontal cortex | UBERON:0000451 | 57.80 | gold quality |
| liver | UBERON:0002107 | 57.70 | gold quality |
| right atrium auricular region | UBERON:0006631 | 57.32 | gold quality |
| adrenal tissue | UBERON:0018303 | 57.27 | gold quality |
| right coronary artery | UBERON:0001625 | 56.80 | gold quality |
| left coronary artery | UBERON:0001626 | 56.28 | gold quality |
| blood | UBERON:0000178 | 56.15 | gold quality |
| tibial artery | UBERON:0007610 | 55.63 | gold quality |
| popliteal artery | UBERON:0002250 | 55.57 | gold quality |
| calcaneal tendon | UBERON:0003701 | 55.52 | gold quality |
| muscle of leg | UBERON:0001383 | 55.35 | gold quality |
| monocyte | CL:0000576 | 55.19 | gold quality |
| thoracic aorta | UBERON:0001515 | 54.40 | gold quality |
| ascending aorta | UBERON:0001496 | 54.27 | gold quality |
| lymph node | UBERON:0000029 | 54.23 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 53.82 | gold quality |
| pancreas | UBERON:0001264 | 53.56 | gold quality |
| gastrocnemius | UBERON:0001388 | 53.55 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.33 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 1)
- rescue assays demonstrated the function of SP1-SYNE1-AS1 axis in Cardiac hypertrophy (CH). In conclusion, SP1-induced upregulation of lncRNA SYNE1-AS1 promoted CH via miR-525-5p/SP1 axis. (PMID:30652310)
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.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4, autosomal dominant