OR6C6

Olfactory receptor family 6 subfamily C member 6 A6NF89 OR6C6_HUMAN
Protein Coding Chr 12 12q13.2 Swiss-Prot reviewed Entrez 283365
Mutations
297
CL 62 · Tissue 220
Samples
272
CL 59 · Tissue 208
Peptides
193
unique mutant peptides
Transcripts
1
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

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.

TotalCell lineTissue
Mutations29762220
Samples27259208
Peptides19335156

Function

OR6C6 · Olfactory receptor family 6 subfamily C member 6

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. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

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.

TranscriptUniProtMutationsPeptides
ENST00000358433 A6NF89 297 193

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q13.2
Entrez ID

Recurrent Mutations

All 193 amino-acid changes on canonical ENST00000358433 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

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 OR6C6 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in OR6C6 – 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 typeCell linesTissue samples
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
9/42 21%
10/612 2%
Melanoma
7/210 3%
44/1899 2%
Other Solid Cancers
1/94 1%
34/1515 2%
Squamous Cell Lung Carcinoma
0/57 0%
9/810 1%
Osteosarcoma
2/45 4%
0/166 0%
Colorectal Carcinoma
9/143 6%
22/3239 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Non-Small Cell Lung Carcinoma
2/304 1%
12/1390 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Glioma
0/52 0%
13/2127 1%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Other Sarcomas
2/69 3%
2/699 0%
Ovarian Carcinoma
3/109 3%
2/998 0%
Mesothelioma
0/62 0%
1/165 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Head and Neck Carcinoma
2/85 2%
5/1574 0%
Pancreatic Carcinoma
2/89 2%
5/1611 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Kidney Carcinoma
3/85 4%
2/1862 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
4/2550 0%
Medulloblastoma
0/0 0%
1/450 0%
Neuroblastoma
2/87 2%
1/1331 0%
Breast Carcinoma
0/144 0%
7/3264 0%
Non-Cancerous
1/104 1%
0/830 0%

Mutation Distribution

Where OR6C6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in OR6C6 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 297 mutations in OR6C6

About the mutation list
Mutations

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.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide