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 | 4,767 | 646 | 4,099 |
| Samples | 1,312 | 256 | 1,048 |
| Peptides | 1,232 | 216 | 1,046 |
Function
TEX15 · Testis expressed 15, meiosis and synapsis associated
This gene encodes a protein that is required for DNA double-strand break repair, chromosome synapsis, and meiotic recombination in spermatocytes. Male mice with a knockout of the orthologous gene are viable but sterile. Loss-of-function mutations in the orthologous mouse gene cause early meiotic arrest in spermatocytes, before the mid-pachytene stage. Naturally occurring mutations in this gene are associated with nonobstructive azoospermia. [provided by RefSeq, Apr 2017].
Isoforms & Proteins
3 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.
| Transcript | UniProt | Mutations | Peptides |
|---|---|---|---|
| ENST00000643185 | A0A2R8Y358* | 1,721 | 1,226 |
| ENST00000638951 | A0A1W2PS94* | 1,543 | 1,157 |
| ENST00000256246 | Q9BXT5 | 1,503 | 1,122 |
Gene Properties
Recurrent Mutations
All 1122 amino-acid changes on canonical ENST00000256246 · 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 TEX15 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in TEX15 – 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 | 11/40 28% | 0/0 0% |
| Chronic Myelogenous Leukemia | 6/25 24% | 0/0 0% |
| Melanoma | 25/210 12% | 170/1899 9% |
| Endometrial Carcinoma | 11/42 26% | 47/612 8% |
| Unknown | 1/10 10% | 2/29 7% |
| Non-Small Cell Lung Carcinoma | 35/304 12% | 78/1390 6% |
| Other Solid Cancers | 5/94 5% | 96/1515 6% |
| Acute Myeloid Leukemia | 5/90 6% | 0/0 0% |
| Glioblastoma | 5/98 5% | 0/0 0% |
| Hodgkins Lymphoma | 4/16 25% | 3/122 2% |
| Cervical Carcinoma | 2/35 6% | 20/422 5% |
| Squamous Cell Lung Carcinoma | 6/57 11% | 35/810 4% |
| Bladder Carcinoma | 3/58 5% | 44/956 5% |
| Colorectal Carcinoma | 26/143 18% | 111/3239 3% |
| T-Cell Non-Hodgkins Lymphoma | 1/26 4% | 0/0 0% |
| Small Cell Lung Carcinoma | 1/9 11% | 24/752 3% |
| Neuroendocrine Tumour | 15/154 10% | 8/577 1% |
| Germ Cell Tumour | 4/25 16% | 2/169 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 4/133 3% |
| Gastric Carcinoma | 6/74 8% | 48/1809 3% |
| Head and Neck Carcinoma | 4/85 5% | 37/1574 2% |
| Hepatocellular Carcinoma | 3/46 7% | 46/2210 2% |
| Esophageal Squamous Cell Carcinoma | 9/51 18% | 46/2550 2% |
| Esophageal Carcinoma | 3/23 13% | 13/769 2% |
| Plasma Cell Myeloma | 1/44 2% | 6/305 2% |
| Rhabdomyosarcoma | 2/33 6% | 2/171 1% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Ovarian Carcinoma | 5/109 5% | 15/998 2% |
| Other Sarcomas | 10/69 14% | 3/699 0% |
| Glioma | 0/52 0% | 33/2127 2% |
Mutation Distribution
Where TEX15 is mutated · all tissues, split by cell line vs tissue
How many mutations in TEX15 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 50 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 4,767 mutations in TEX15
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 |
|---|