CLLU1
gene geneOn this page
Summary
CLLU1 (chronic lymphocytic leukemia up-regulated 1, HGNC:29841) is a long non-coding RNA gene on chromosome 12q22.
Expression of this gene has been shown to be upregulated in some individuals with chronic lymphocytic leukemia (CLL), and has been used for prognostic and diagnostic purposes. This gene was originally identified as a human-specific putative protein-coding gene due to the presence of a peptide (PAp00140670, HIIYSTFLSK) that could have supported translation at this locus. This peptide is not present in more recent builds of PeptideAtlas, and the presence of a protein product at this locus has not been independently verified. For this reason, this gene is being represented as non-coding. Sequence comparisons to other primates indicates that no other primate is predicted to contain an open reading frame.
Source: NCBI Gene 574028 — RefSeq curated summary.
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:29841 |
| Approved symbol | CLLU1 |
| Name | chronic lymphocytic leukemia up-regulated 1 |
| Location | 12q22 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000257127 |
| Ensembl biotype | lncRNA |
| OMIM | 616988 |
| Entrez | 574028 |
| RNAcentral | URS00008B6E4E — lncRNA, 2831 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 5 — 3 lncRNA, 2 retained_intron
ENST00000378485, ENST00000472839, ENST00000512817, ENST00000586526, ENST00000589406
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000378485 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001477676 | 92429034 | 92430954 |
| ENSE00001477677 | 92423959 | 92425934 |
Expression profiles
Bgee: expression breadth broad, 71 present calls, max score 71.94.
Top tissues by expression
71 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 71.94 | silver quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 59.39 | gold quality |
| corpus callosum | UBERON:0002336 | 56.72 | gold quality |
| calcaneal tendon | UBERON:0003701 | 53.02 | gold quality |
| monocyte | CL:0000576 | 52.72 | silver quality |
| endometrium | UBERON:0001295 | 52.24 | silver quality |
| muscle of leg | UBERON:0001383 | 51.19 | gold quality |
| gastrocnemius | UBERON:0001388 | 51.05 | gold quality |
| urinary bladder | UBERON:0001255 | 50.37 | silver quality |
| liver | UBERON:0002107 | 50.26 | silver quality |
| anterior cingulate cortex | UBERON:0009835 | 50.25 | gold quality |
| lymph node | UBERON:0000029 | 48.98 | silver quality |
| blood | UBERON:0000178 | 48.88 | gold quality |
| cerebellar cortex | UBERON:0002129 | 46.77 | silver quality |
| metanephros cortex | UBERON:0010533 | 46.73 | gold quality |
| cortex of kidney | UBERON:0001225 | 46.30 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 46.26 | silver quality |
| vermiform appendix | UBERON:0001154 | 45.80 | silver quality |
| tonsil | UBERON:0002372 | 45.68 | gold quality |
| left coronary artery | UBERON:0001626 | 44.94 | gold quality |
| tibial nerve | UBERON:0001323 | 44.62 | silver quality |
| skin of leg | UBERON:0001511 | 44.19 | silver quality |
| ectocervix | UBERON:0012249 | 43.97 | gold quality |
| pancreas | UBERON:0001264 | 43.71 | silver quality |
| islet of Langerhans | UBERON:0000006 | 43.27 | silver quality |
| heart | UBERON:0000948 | 43.02 | silver quality |
| placenta | UBERON:0001987 | 43.02 | silver quality |
| esophagus mucosa | UBERON:0002469 | 42.81 | silver quality |
| esophagus | UBERON:0001043 | 42.70 | silver quality |
| body of pancreas | UBERON:0001150 | 42.45 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 5.55 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 11)
- CLLU1 is the first disease-specific gene identified in chronic lymphocytic leukemia. (PMID:16339396)
- CLLU1 has a role in progression of chronic lymphocytic leukemia (PMID:17284524)
- The expression levels of CLLU1 were significantly increased in B + C CLL patients at Binet stage compared with those at Binet stage A (P = 0.005). (PMID:17786715)
- CLLU1 expression was significantly associated with clinical stage and CD38 expression in chronic lymphocytic leukemia. (PMID:18457263)
- The CLLU1 expression level is a stable and inherent feature of the chronic lymphocytic leukemia clone (PMID:19212335)
- CLLU1 is a novel human-specific protein-coding gene. (PMID:19726446)
- Assessment of blood CLLU1 levels can be used as a reliable marker of tumor burden and has the potential to complement currently used techniques for minimal residual disease monitoring in patients with chronic lymphocytic leukemia. (PMID:21323738)
- Analysis of CLLU1 expression is a rapid and reliable tool that may facilitate the diagnosis of mature B-cell neoplasms especially in inconclusive cases. (PMID:22738889)
- the level of CLLU1 mRNA expression provided prognostic information in patients with CLL. (PMID:22899580)
- in this paper we have showed that evolutionary new genes DCD1(Dermicidin), LINC00309 and CLLU1 have tumor-specific expression profile (PMID:30463107)
- The Impact and Prognostic Significance of Chronic Lymphocytic Leukemia Upregulated 1 (CLLU1) Gene Expression in Patients with Chronic Lymphocytic Leukemia: A Single Center Experience. (PMID:31589746)
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
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.