Stats by Source
Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)
Total = all mutations for this gene across every source.
Cell line = COSMIC Cell Lines Project + DepMap + PubMed.
Tissue = COSMIC primary-tissue (patient tumour) samples.
Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.
| Total | Cell line | Tissue | |
|---|---|---|---|
| Mutations | 1,010 | 119 | 872 |
| Samples | 484 | 70 | 406 |
| Peptides | 373 | 53 | 321 |
Function
TIMELESS · Timeless circadian regulator
The protein encoded by this gene is highly conserved and is involved in cell survival after damage or stress, increase in DNA polymerase epsilon activity, maintenance of telomere length, and epithelial cell morphogenesis. The encoded protein also plays a role in the circadian rhythm autoregulatory loop, interacting with the PERIOD genes (PER1, PER2, and PER3) and others to downregulate activation of PER1 by CLOCK/ARNTL. Changes in this gene or its expression may promote prostate cancer, lung cancer, breast cancer, and mental disorders. [provided by RefSeq, Feb 2014].
Isoforms & Proteins
2 transcripts · UniProt mapping is sequence-verified (AA-safe)
Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.
The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.
Counts are mutations and unique mutant peptides on each transcript.
Gene Properties
Recurrent Mutations
All 364 amino-acid changes on canonical ENST00000553532 · needle height = samples · drag the mini-map to zoom
A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).
X-axis = amino-acid position in the protein.
Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.
The most recurrent changes are labelled; hover any needle for the change, position and counts.
Mutation frequency across cancer types
% of samples with a missense/complex mutation in TIMELESS · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in TIMELESS – counted as distinct samples (a sample counts once no matter how many mutations it has).
Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.
| Cancer type | Cell lines | Tissue samples |
|---|---|---|
| T-Lymphoblastic Leukemia | 5/40 12% | 0/0 0% |
| Chronic Myelogenous Leukemia | 2/25 8% | 0/0 0% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 7/133 5% |
| Endometrial Carcinoma | 4/42 10% | 23/612 4% |
| Unknown | 0/10 0% | 1/29 3% |
| Melanoma | 5/210 2% | 44/1899 2% |
| Colorectal Carcinoma | 14/143 10% | 63/3239 2% |
| Acute Myeloid Leukemia | 2/90 2% | 0/0 0% |
| Bladder Carcinoma | 3/58 5% | 19/956 2% |
| Hodgkins Lymphoma | 0/16 0% | 3/122 2% |
| Gastric Carcinoma | 2/74 3% | 32/1809 2% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 14/810 2% |
| Rhabdomyosarcoma | 3/33 9% | 0/171 0% |
| Other Solid Cancers | 0/94 0% | 23/1515 2% |
| Non-Small Cell Lung Carcinoma | 5/304 2% | 18/1390 1% |
| Burkitts Lymphoma | 0/32 0% | 3/196 2% |
| Cervical Carcinoma | 0/35 0% | 6/422 1% |
| Other Sarcomas | 4/69 6% | 6/699 1% |
| Neuroendocrine Tumour | 3/154 2% | 6/577 1% |
| Plasma Cell Myeloma | 4/44 9% | 0/305 0% |
| Chondrosarcoma | 0/14 0% | 1/75 1% |
| Ovarian Carcinoma | 1/109 1% | 9/998 1% |
| Head and Neck Carcinoma | 1/85 1% | 14/1574 1% |
| Hepatocellular Carcinoma | 3/46 7% | 17/2210 1% |
| Glioma | 0/52 0% | 18/2127 1% |
| Esophageal Carcinoma | 0/23 0% | 6/769 1% |
| Thyroid Gland Carcinoma | 1/45 2% | 10/1592 1% |
| Esophageal Squamous Cell Carcinoma | 1/51 2% | 16/2550 1% |
| Non-Cancerous | 0/104 0% | 6/830 1% |
| Ewings Sarcoma | 0/63 0% | 2/262 1% |
Mutation Distribution
Where TIMELESS is mutated · all tissues, split by cell line vs tissue
How many mutations in TIMELESS were found in each tissue, across the whole database.
Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.
This shows the cancer-context where this gene is recurrently altered.
GTEx Expression
Median TPM across 54 healthy tissues
Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.
Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.
Scroll or drag the mini-axis below the chart to browse all tissues.
Mutations
All 1,010 mutations in TIMELESS
Every mutation record for this gene, across all samples and sources.
The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).
Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.
| ID | Sample | Transcript | AA Change | CDS | Type | Source | Mutant Peptide | Wild-type Peptide |
|---|