OR5AC2

Olfactory receptor family 5 subfamily AC member 2 Q9NZP5 O5AC2_HUMAN
Protein Coding Chr 3 3q11.2 Swiss-Prot reviewed Entrez 81050
Mutations
341
CL 57 · Tissue 280
Samples
318
CL 52 · Tissue 262
Peptides
203
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
Mutations34157280
Samples31852262
Peptides20335171

Function

OR5AC2 · Olfactory receptor family 5 subfamily AC member 2

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
ENST00000358642 Q9NZP5 341 203

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q11.2
Entrez ID
Aliases
HSA1

Recurrent Mutations

All 203 amino-acid changes on canonical ENST00000358642 · 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 OR5AC2 · 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 OR5AC2 – 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-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Melanoma
2/210 1%
65/1899 3%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Squamous Cell Lung Carcinoma
3/57 5%
18/810 2%
Other Solid Cancers
0/94 0%
30/1515 2%
Non-Small Cell Lung Carcinoma
13/304 4%
18/1390 1%
Endometrial Carcinoma
2/42 5%
8/612 1%
Colorectal Carcinoma
8/143 6%
33/3239 1%
Bladder Carcinoma
0/58 0%
10/956 1%
Mesothelioma
2/62 3%
0/165 0%
Gastric Carcinoma
1/74 1%
14/1809 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Small Cell Lung Carcinoma
1/9 11%
4/752 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Ovarian Carcinoma
2/109 2%
3/998 0%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Other Sarcomas
3/69 4%
0/699 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Non-Cancerous
0/104 0%
3/830 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Glioma
0/52 0%
6/2127 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
B-Lymphoblastic Leukemia
3/55 5%
3/2640 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Breast Carcinoma
1/144 1%
4/3264 0%
Kidney Carcinoma
0/85 0%
3/1862 0%

Mutation Distribution

Where OR5AC2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in OR5AC2 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

GTEx Portal ↗
About the expression data
GTEx Expression

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 341 mutations in OR5AC2

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