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 | 1,804 | 204 | 1,593 |
| Samples | 424 | 75 | 346 |
| Peptides | 365 | 56 | 319 |
Function
SELE · Selectin E
The protein encoded by this gene is found in cytokine-stimulated endothelial cells and is thought to be responsible for the accumulation of blood leukocytes at sites of inflammation by mediating the adhesion of cells to the vascular lining. It exhibits structural features such as the presence of lectin- and EGF-like domains followed by short consensus repeat (SCR) domains that contain 6 conserved cysteine residues. These proteins are part of the selectin family of cell adhesion molecules. Adhesion molecules participate in the interaction between leukocytes and the endothelium and appear to be involved in the pathogenesis of atherosclerosis. [provided by RefSeq, Jul 2008].
Isoforms & Proteins
5 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 316 amino-acid changes on canonical ENST00000333360 · 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 SELE · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in SELE – 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 |
|---|---|---|
| Chronic Myelogenous Leukemia | 3/25 12% | 0/0 0% |
| Melanoma | 14/210 7% | 94/1899 5% |
| Acute Monocytic Leukemia | 0/1 0% | 1/25 4% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 4/133 3% |
| Endometrial Carcinoma | 3/42 7% | 13/612 2% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Non-Small Cell Lung Carcinoma | 6/304 2% | 23/1390 2% |
| Squamous Cell Lung Carcinoma | 3/57 5% | 10/810 1% |
| Rhabdomyosarcoma | 0/33 0% | 3/171 2% |
| Other Solid Cancers | 0/94 0% | 23/1515 2% |
| Cervical Carcinoma | 2/35 6% | 4/422 1% |
| Head and Neck Carcinoma | 5/85 6% | 15/1574 1% |
| Gastric Carcinoma | 8/74 11% | 14/1809 1% |
| Neuroendocrine Tumour | 5/154 3% | 3/577 1% |
| Glioma | 0/52 0% | 23/2127 1% |
| Colorectal Carcinoma | 5/143 4% | 30/3239 1% |
| Bladder Carcinoma | 0/58 0% | 10/956 1% |
| Ewings Sarcoma | 2/63 3% | 1/262 0% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Plasma Cell Myeloma | 2/44 5% | 1/305 0% |
| Small Cell Lung Carcinoma | 0/9 0% | 6/752 1% |
| Esophageal Carcinoma | 0/23 0% | 6/769 1% |
| Neuroblastoma | 3/87 3% | 4/1331 0% |
| Ovarian Carcinoma | 0/109 0% | 5/998 0% |
| Medulloblastoma | 0/0 0% | 2/450 0% |
| Biliary Tract Carcinoma | 3/54 6% | 1/950 0% |
| Breast Carcinoma | 2/144 1% | 11/3264 0% |
| Kidney Carcinoma | 0/85 0% | 7/1862 0% |
| B-Lymphoblastic Leukemia | 4/55 7% | 5/2640 0% |
| Non-Cancerous | 0/104 0% | 3/830 0% |
Mutation Distribution
Where SELE is mutated · all tissues, split by cell line vs tissue
How many mutations in SELE 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 53 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 1,804 mutations in SELE
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 |
|---|