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 | 454 | 69 | 376 |
| Samples | 435 | 69 | 359 |
| Peptides | 285 | 43 | 251 |
Function
OR10X1 · Olfactory receptor family 10 subfamily X member 1
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. This olfactory receptor gene is a segregating pseudogene, where some individuals have an allele that encodes a functional olfactory receptor, while other individuals have an allele encoding a protein that is predicted to be non-functional. [provided by RefSeq, Jun 2015].
Isoforms & Proteins
1 transcript · 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 |
|---|---|---|---|
| ENST00000623167 | Q8NGY0 | 454 | 285 |
Gene Properties
Recurrent Mutations
All 285 amino-acid changes on canonical ENST00000623167 · 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 OR10X1 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in OR10X1 – 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 |
|---|---|---|
| Gastrointestinal Stromal Tumour | 0/0 0% | 6/133 5% |
| Melanoma | 7/210 3% | 75/1899 4% |
| Endometrial Carcinoma | 1/42 2% | 22/612 4% |
| Thymic Epithelial Tumor | 0/0 0% | 1/39 3% |
| Non-Small Cell Lung Carcinoma | 6/304 2% | 35/1390 3% |
| Neuroendocrine Tumour | 10/154 6% | 7/577 1% |
| Other Solid Cancers | 3/94 3% | 32/1515 2% |
| Esophageal Carcinoma | 3/23 13% | 12/769 2% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Squamous Cell Lung Carcinoma | 2/57 4% | 14/810 2% |
| Gastric Carcinoma | 2/74 3% | 26/1809 1% |
| Pheochromocytoma and Paraganglioma | 0/0 0% | 1/71 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 9/752 1% |
| Colorectal Carcinoma | 9/143 6% | 29/3239 1% |
| Cervical Carcinoma | 1/35 3% | 3/422 1% |
| Biliary Tract Carcinoma | 1/54 2% | 7/950 1% |
| Head and Neck Carcinoma | 2/85 2% | 10/1574 1% |
| Bladder Carcinoma | 1/58 2% | 6/956 1% |
| Hepatocellular Carcinoma | 1/46 2% | 14/2210 1% |
| Esophageal Squamous Cell Carcinoma | 5/51 10% | 12/2550 0% |
| Pancreatic Carcinoma | 1/89 1% | 8/1611 0% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Breast Carcinoma | 5/144 3% | 11/3264 0% |
| Osteosarcoma | 1/45 2% | 0/166 0% |
| Other Sarcomas | 1/69 1% | 2/699 0% |
| Ovarian Carcinoma | 1/109 1% | 3/998 0% |
| Glioma | 2/52 4% | 5/2127 0% |
| Wilms Tumour | 0/5 0% | 1/474 0% |
| Non-Cancerous | 0/104 0% | 2/830 0% |
| Prostate Carcinoma | 0/13 0% | 4/2105 0% |
Mutation Distribution
Where OR10X1 is mutated · all tissues, split by cell line vs tissue
How many mutations in OR10X1 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 1 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 454 mutations in OR10X1
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 |
|---|