OR10J5

Olfactory receptor family 10 subfamily J member 5 Q8NHC4 O10J5_HUMAN
Protein Coding Chr 1 1q23.2 Swiss-Prot reviewed Entrez 127385
Mutations
336
CL 74 · Tissue 259
Samples
321
CL 69 · Tissue 249
Peptides
207
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
Mutations33674259
Samples32169249
Peptides20741178

Function

OR10J5 · Olfactory receptor family 10 subfamily J member 5

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
ENST00000334857 Q8NHC4 336 207

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q23.2
Entrez ID
Aliases
MOR23OLFR16OR1-28

Recurrent Mutations

All 207 amino-acid changes on canonical ENST00000334857 · 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 OR10J5 · 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 OR10J5 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Melanoma
9/210 4%
59/1899 3%
Non-Small Cell Lung Carcinoma
15/304 5%
24/1390 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Endometrial Carcinoma
5/42 12%
9/612 1%
Squamous Cell Lung Carcinoma
1/57 2%
14/810 2%
Other Solid Cancers
2/94 2%
20/1515 1%
Neuroendocrine Tumour
5/154 3%
2/577 0%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Gastric Carcinoma
3/74 4%
14/1809 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Colorectal Carcinoma
4/143 3%
25/3239 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Bladder Carcinoma
0/58 0%
7/956 1%
Other Sarcomas
4/69 6%
0/699 0%
Osteosarcoma
1/45 2%
0/166 0%
Cervical Carcinoma
2/35 6%
0/422 0%
Non-Cancerous
0/104 0%
4/830 0%
Esophageal Squamous Cell Carcinoma
3/51 6%
6/2550 0%
Breast Carcinoma
2/144 1%
10/3264 0%
Glioma
1/52 2%
6/2127 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Neuroblastoma
0/87 0%
3/1331 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Ovarian Carcinoma
0/109 0%
2/998 0%

Mutation Distribution

Where OR10J5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in OR10J5 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 336 mutations in OR10J5

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