AP4B1-AS1
gene geneOn this page
Summary
AP4B1-AS1 (AP4B1 antisense RNA 1, HGNC:44114) is a long non-coding RNA gene on chromosome 1p13.2.
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:44114 |
| Approved symbol | AP4B1-AS1 |
| Name | AP4B1 antisense RNA 1 |
| Location | 1p13.2 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000226167 |
| Ensembl biotype | lncRNA |
| Entrez | 100287722 |
| RNAcentral | URS000036AE88 — lncRNA, 1734 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 16 — 16 lncRNA
ENST00000418238, ENST00000419536, ENST00000429398, ENST00000448199, ENST00000664434, ENST00000702317, ENST00000717022, ENST00000836797, ENST00000836798, ENST00000836799, ENST00000836800, ENST00000836801, ENST00000836802, ENST00000836803, ENST00000836804, ENST00000836805
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000418238 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00004256624 | 113814387 | 113814634 |
| ENSE00004256625 | 113812579 | 113812825 |
Expression profiles
Bgee: expression breadth ubiquitous, 130 present calls, max score 79.30.
FANTOM5 (CAGE): breadth broad, TPM avg 1.6862 / max 47.3639, expressed in 420 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 4725 | 1.6862 | 420 |
Top tissues by expression
130 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 79.30 | gold quality |
| granulocyte | CL:0000094 | 74.47 | gold quality |
| lymph node | UBERON:0000029 | 71.13 | gold quality |
| duodenum | UBERON:0002114 | 70.68 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 70.67 | gold quality |
| bone marrow | UBERON:0002371 | 70.40 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 70.31 | gold quality |
| cerebellar cortex | UBERON:0002129 | 70.28 | gold quality |
| body of pancreas | UBERON:0001150 | 70.27 | gold quality |
| vermiform appendix | UBERON:0001154 | 70.23 | gold quality |
| cerebellum | UBERON:0002037 | 70.15 | gold quality |
| endometrium | UBERON:0001295 | 69.55 | gold quality |
| colonic epithelium | UBERON:0000397 | 69.01 | silver quality |
| spleen | UBERON:0002106 | 68.86 | gold quality |
| blood | UBERON:0000178 | 68.37 | gold quality |
| rectum | UBERON:0001052 | 68.16 | gold quality |
| monocyte | CL:0000576 | 67.79 | gold quality |
| cortical plate | UBERON:0005343 | 67.49 | gold quality |
| leukocyte | CL:0000738 | 67.40 | gold quality |
| bone marrow cell | CL:0002092 | 67.27 | silver quality |
| small intestine Peyer’s patch | UBERON:0003454 | 67.17 | gold quality |
| ganglionic eminence | UBERON:0004023 | 67.14 | gold quality |
| small intestine | UBERON:0002108 | 67.12 | gold quality |
| transverse colon | UBERON:0001157 | 67.09 | gold quality |
| right ovary | UBERON:0002118 | 66.12 | gold quality |
| left ovary | UBERON:0002119 | 65.87 | gold quality |
| ovary | UBERON:0000992 | 65.53 | gold quality |
| intestine | UBERON:0000160 | 65.52 | gold quality |
| body of stomach | UBERON:0001161 | 65.49 | gold quality |
| fundus of stomach | UBERON:0001160 | 65.38 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.06 |
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): hereditary spastic paraplegia 47