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 | 449 | 72 | 377 |
| Samples | 355 | 72 | 283 |
| Peptides | 237 | 44 | 204 |
Function
OR1S1 · Olfactory receptor family 1 subfamily S 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 |
|---|---|---|---|
| ENST00000641544 | A0A286YF57* | 449 | 237 |
Gene Properties
Recurrent Mutations
All 237 amino-acid changes on canonical ENST00000641544 · 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 OR1S1 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in OR1S1 – 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 |
|---|---|---|
| Glioblastoma | 4/98 4% | 0/0 0% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 5/133 4% |
| Melanoma | 6/210 3% | 44/1899 2% |
| Acute Myeloid Leukemia | 2/90 2% | 0/0 0% |
| Squamous Cell Lung Carcinoma | 4/57 7% | 15/810 2% |
| Endometrial Carcinoma | 1/42 2% | 13/612 2% |
| Other Solid Cancers | 5/94 5% | 22/1515 1% |
| Non-Small Cell Lung Carcinoma | 4/304 1% | 24/1390 2% |
| Cervical Carcinoma | 0/35 0% | 7/422 2% |
| Colorectal Carcinoma | 15/143 10% | 29/3239 1% |
| Neuroendocrine Tumour | 4/154 3% | 4/577 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 8/752 1% |
| Osteosarcoma | 2/45 4% | 0/166 0% |
| Gastric Carcinoma | 2/74 3% | 15/1809 1% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Mesothelioma | 2/62 3% | 0/165 0% |
| Plasma Cell Myeloma | 0/44 0% | 3/305 1% |
| Ovarian Carcinoma | 4/109 4% | 4/998 0% |
| Medulloblastoma | 0/0 0% | 3/450 1% |
| Other Sarcomas | 2/69 3% | 3/699 0% |
| Esophageal Carcinoma | 0/23 0% | 5/769 1% |
| Bladder Carcinoma | 0/58 0% | 6/956 1% |
| Hepatocellular Carcinoma | 0/46 0% | 13/2210 1% |
| Glioma | 2/52 4% | 10/2127 0% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 12/2550 0% |
| Head and Neck Carcinoma | 1/85 1% | 6/1574 0% |
| Non-Cancerous | 1/104 1% | 2/830 0% |
| B-Cell Non-Hodgkins Lymphoma | 2/88 2% | 5/2534 0% |
| Kidney Carcinoma | 2/85 2% | 3/1862 0% |
Mutation Distribution
Where OR1S1 is mutated · all tissues, split by cell line vs tissue
How many mutations in OR1S1 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.
Mutations
All 449 mutations in OR1S1
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 |
|---|