UVRAG-DT
gene geneOn this page
Also known as LOC100506113
Summary
UVRAG-DT (UVRAG divergent transcript, HGNC:53952) is a long non-coding RNA gene on chromosome 11q13.5.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:53952 |
| Approved symbol | UVRAG-DT |
| Name | UVRAG divergent transcript |
| Location | 11q13.5 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | LOC100506113 |
| Ensembl gene | ENSG00000255507 |
| Entrez | 100506113 |
| RNAcentral | URS0000A7649D — lncRNA, 689 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 0
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
None — 0 exons
Expression profiles
Bgee: expression breadth ubiquitous, 154 present calls, max score 89.62.
Top tissues by expression
246 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| left testis | UBERON:0004533 | 89.62 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 89.03 | gold quality |
| right testis | UBERON:0004534 | 88.61 | gold quality |
| testis | UBERON:0000473 | 86.51 | gold quality |
| skin of leg | UBERON:0001511 | 77.55 | gold quality |
| sperm | CL:0000019 | 77.28 | silver quality |
| skin of abdomen | UBERON:0001416 | 74.69 | gold quality |
| buccal mucosa cell | CL:0002336 | 72.72 | silver quality |
| zone of skin | UBERON:0000014 | 72.09 | gold quality |
| tibialis anterior | UBERON:0001385 | 69.69 | silver quality |
| hindlimb stylopod muscle | UBERON:0004252 | 69.49 | gold quality |
| right uterine tube | UBERON:0001302 | 68.22 | gold quality |
| ganglionic eminence | UBERON:0004023 | 66.86 | gold quality |
| pancreatic ductal cell | CL:0002079 | 66.50 | silver quality |
| omental fat pad | UBERON:0010414 | 65.95 | gold quality |
| cortical plate | UBERON:0005343 | 65.94 | gold quality |
| peritoneum | UBERON:0002358 | 65.88 | gold quality |
| ventricular zone | UBERON:0003053 | 65.63 | gold quality |
| monocyte | CL:0000576 | 65.53 | gold quality |
| ileal mucosa | UBERON:0000331 | 65.26 | silver quality |
| stromal cell of endometrium | CL:0002255 | 65.12 | gold quality |
| leukocyte | CL:0000738 | 64.70 | gold quality |
| adipose tissue of abdominal region | UBERON:0007808 | 64.56 | gold quality |
| bone marrow cell | CL:0002092 | 64.43 | silver quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 64.29 | gold quality |
| right lobe of liver | UBERON:0001114 | 64.23 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 63.82 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 60.48 | gold quality |
| blood | UBERON:0000178 | 59.52 | gold quality |
| gall bladder | UBERON:0002110 | 59.15 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-9543 | yes | 14.97 |
| E-ANND-3 | no | 2.29 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Protein
Protein identifiers
Canonical reviewed UniProt: None (reviewed: )
All UniProt accessions (0):
RefSeq proteins (0): (*=MANE)
Domains & families (InterPro)
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chr11q13
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (0):
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
472 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 11:75796513:G:GT | donor_gain | 1.0000 |
| 11:75796529:GGAG:G | donor_gain | 1.0000 |
| 11:75796530:GAG:G | donor_gain | 1.0000 |
| 11:75796530:GAGG:G | donor_gain | 1.0000 |
| 11:75796531:AGGTA:A | donor_loss | 1.0000 |
| 11:75796532:GGTA:G | donor_loss | 1.0000 |
| 11:75796533:GT:G | donor_loss | 1.0000 |
| 11:75796534:T:A | donor_loss | 1.0000 |
| 11:75797153:CTCA:C | acceptor_loss | 1.0000 |
| 11:75797156:A:AG | acceptor_gain | 1.0000 |
| 11:75797156:A:AT | acceptor_loss | 1.0000 |
| 11:75797156:AG:A | acceptor_gain | 1.0000 |
| 11:75797157:G:A | acceptor_loss | 1.0000 |
| 11:75797157:G:GC | acceptor_gain | 1.0000 |
| 11:75797157:GG:G | acceptor_gain | 1.0000 |
| 11:75797157:GGT:G | acceptor_gain | 1.0000 |
| 11:75797157:GGTA:G | acceptor_gain | 1.0000 |
| 11:75797157:GGTAT:G | acceptor_gain | 1.0000 |
| 11:75797329:ATGG:A | donor_gain | 1.0000 |
| 11:75797330:TGG:T | donor_gain | 1.0000 |
| 11:75797330:TGGG:T | donor_loss | 1.0000 |
| 11:75797331:GG:G | donor_gain | 1.0000 |
| 11:75797331:GGG:G | donor_gain | 1.0000 |
| 11:75797331:GGGT:G | donor_loss | 1.0000 |
| 11:75797332:GG:G | donor_gain | 1.0000 |
| 11:75797333:G:C | donor_loss | 1.0000 |
| 11:75797333:G:GG | donor_gain | 1.0000 |
| 11:75797334:T:A | donor_loss | 1.0000 |
| 11:75798224:CAG:C | acceptor_gain | 1.0000 |
| 11:75798225:A:AG | acceptor_gain | 1.0000 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000794020 (11:75813300 C>A,T), RS1001583691 (11:75814308 A>G), RS1001874756 (11:75816191 GTA>G,GTATA), RS1002326552 (11:75815412 G>A,C), RS1003158238 (11:75815071 GC>G), RS1003590539 (11:75816435 T>G), RS1004424924 (11:75815393 G>A,C,T), RS1004566653 (11:75813350 G>A), RS1004845275 (11:75815226 C>G,T), RS1005881723 (11:75816760 C>T), RS1006006127 (11:75816702 TCCA>T), RS1007005365 (11:75815341 T>C,G), RS1007230789 (11:75813401 C>A), RS1007262072 (11:75813908 G>T), RS1008228540 (11:75814852 C>T)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 0 entries
CTD chemical–gene interactions
3 total (human), top 3 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| S-(1,2-dichlorovinyl)cysteine | decreases expression, decreases reaction | 1 |
| Lipopolysaccharides | decreases expression, decreases reaction | 1 |
| Tobacco Smoke Pollution | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.