SYNGAP1-AS1
gene geneOn this page
Also known as SYNGAP1-AS
Summary
SYNGAP1-AS1 (SYNGAP1 antisense RNA 1, HGNC:53831) is a long non-coding RNA gene on chromosome 6p21.32.
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:53831 |
| Approved symbol | SYNGAP1-AS1 |
| Name | SYNGAP1 antisense RNA 1 |
| Location | 6p21.32 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | SYNGAP1-AS |
| Ensembl gene | ENSG00000274259 |
| Ensembl biotype | lncRNA |
| Entrez | 112390310 |
| RNAcentral | URS00025E34C0 — lncRNA, 448 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 4 — 4 lncRNA
ENST00000614205, ENST00000630418, ENST00000815438, ENST00000815439
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000614205 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00004217437 | 33453662 | 33454470 |
Expression profiles
Bgee: expression breadth ubiquitous, 133 present calls, max score 93.53.
FANTOM5 (CAGE): breadth broad, TPM avg 0.6370 / max 39.9712, expressed in 364 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 73168 | 0.6370 | 364 |
Top tissues by expression
136 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| thymus | UBERON:0002370 | 93.53 | silver quality |
| sural nerve | UBERON:0015488 | 91.99 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 80.70 | gold quality |
| pituitary gland | UBERON:0000007 | 77.63 | gold quality |
| adenohypophysis | UBERON:0002196 | 74.35 | gold quality |
| colonic epithelium | UBERON:0000397 | 72.05 | gold quality |
| cortical plate | UBERON:0005343 | 71.76 | gold quality |
| right uterine tube | UBERON:0001302 | 70.96 | gold quality |
| bone marrow cell | CL:0002092 | 70.50 | silver quality |
| quadriceps femoris | UBERON:0001377 | 70.45 | gold quality |
| ganglionic eminence | UBERON:0004023 | 69.94 | gold quality |
| ventricular zone | UBERON:0003053 | 68.10 | gold quality |
| cerebellar vermis | UBERON:0004720 | 67.75 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 67.68 | gold quality |
| granulocyte | CL:0000094 | 67.45 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 66.84 | gold quality |
| tonsil | UBERON:0002372 | 66.28 | gold quality |
| heart left ventricle | UBERON:0002084 | 66.22 | gold quality |
| right testis | UBERON:0004534 | 66.14 | gold quality |
| placenta | UBERON:0001987 | 65.73 | gold quality |
| left testis | UBERON:0004533 | 65.52 | gold quality |
| testis | UBERON:0000473 | 65.15 | gold quality |
| prefrontal cortex | UBERON:0000451 | 64.79 | gold quality |
| left ovary | UBERON:0002119 | 64.79 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 64.67 | gold quality |
| ovary | UBERON:0000992 | 64.60 | gold quality |
| right coronary artery | UBERON:0001625 | 64.59 | gold quality |
| thyroid gland | UBERON:0002046 | 64.59 | gold quality |
| right ovary | UBERON:0002118 | 64.48 | gold quality |
| blood | UBERON:0000178 | 64.33 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.46 |
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.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): infantile epileptic-dyskinetic encephalopathy, intellectual disability, autosomal dominant 5