UBOX5-AS1
gene geneOn this page
Summary
UBOX5-AS1 (UBOX5 antisense RNA 1, HGNC:44111) is a long non-coding RNA gene on chromosome 20p13.
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:44111 |
| Approved symbol | UBOX5-AS1 |
| Name | UBOX5 antisense RNA 1 |
| Location | 20p13 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000235958 |
| Ensembl biotype | lncRNA |
| Entrez | 100134015 |
| RNAcentral | URS000075BA4F — lncRNA, 1794 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 5 — 5 lncRNA
ENST00000446537, ENST00000454019, ENST00000840179, ENST00000840180, ENST00000840181
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000446537 — 7 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001602662 | 3111644 | 3111752 |
| ENSE00001649226 | 3106913 | 3107571 |
| ENSE00001770755 | 3109475 | 3109750 |
| ENSE00001774457 | 3150538 | 3150867 |
| ENSE00001783920 | 3110632 | 3110717 |
| ENSE00001789366 | 3110278 | 3110453 |
| ENSE00001797713 | 3136003 | 3136158 |
Expression profiles
Bgee: expression breadth ubiquitous, 132 present calls, max score 83.57.
Top tissues by expression
132 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 83.57 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 81.06 | gold quality |
| sural nerve | UBERON:0015488 | 79.50 | gold quality |
| bone marrow | UBERON:0002371 | 70.48 | gold quality |
| bone marrow cell | CL:0002092 | 70.27 | silver quality |
| blood | UBERON:0000178 | 69.90 | gold quality |
| apex of heart | UBERON:0002098 | 69.35 | gold quality |
| ventricular zone | UBERON:0003053 | 69.21 | gold quality |
| right testis | UBERON:0004534 | 67.24 | gold quality |
| left testis | UBERON:0004533 | 67.00 | gold quality |
| testis | UBERON:0000473 | 66.71 | gold quality |
| colonic epithelium | UBERON:0000397 | 66.70 | silver quality |
| monocyte | CL:0000576 | 65.99 | gold quality |
| granulocyte | CL:0000094 | 65.15 | gold quality |
| cortical plate | UBERON:0005343 | 65.13 | gold quality |
| stromal cell of endometrium | CL:0002255 | 64.20 | gold quality |
| adrenal tissue | UBERON:0018303 | 63.53 | gold quality |
| spleen | UBERON:0002106 | 62.15 | gold quality |
| skin of leg | UBERON:0001511 | 62.05 | gold quality |
| zone of skin | UBERON:0000014 | 61.95 | gold quality |
| skin of abdomen | UBERON:0001416 | 61.92 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 61.89 | gold quality |
| fundus of stomach | UBERON:0001160 | 61.41 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 61.29 | gold quality |
| body of pancreas | UBERON:0001150 | 61.25 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 61.08 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 61.08 | gold quality |
| adrenal gland | UBERON:0002369 | 61.03 | gold quality |
| cerebellum | UBERON:0002037 | 60.98 | gold quality |
| cerebellar cortex | UBERON:0002129 | 60.95 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 2.55 |
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): Leigh syndrome, mitochondrial complex IV deficiency, nuclear type 24