OTOS

Otospiralin Q8NHW6 OTOSP_HUMAN
Protein Coding Chr 2 2q37.3 Swiss-Prot reviewed Entrez 150677
Mutations
131
CL 17 · Tissue 110
Samples
67
CL 11 · Tissue 54
Peptides
48
unique mutant peptides
Transcripts
2
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
Mutations13117110
Samples671154
Peptides48841

Function

OTOS · Otospiralin

Otospiralin is synthesized by nonsensory cells (fibrocytes) of the inner ear, and downregulation of otospiralin in guinea pigs leads to deafness (Lavigne-Rebillard et al., 2003 [PubMed 12687421]).[supplied by OMIM, Mar 2008].

Isoforms & Proteins

2 transcripts · 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
ENST00000319460 Q8NHW6 68 48
ENST00000391989 Q8NHW6 63 45

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q37.3
Entrez ID
Aliases
OTOSP

Recurrent Mutations

All 48 amino-acid changes on canonical ENST00000319460 · 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 OTOS · 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 OTOS – 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
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Melanoma
2/210 1%
13/1899 1%
Endometrial Carcinoma
0/42 0%
4/612 1%
Non-Small Cell Lung Carcinoma
1/304 0%
5/1390 0%
Glioma
0/52 0%
6/2127 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Colorectal Carcinoma
0/143 0%
7/3239 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
Hepatocellular Carcinoma
1/46 2%
1/2210 0%
Breast Carcinoma
0/144 0%
3/3264 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Neuroblastoma
0/87 0%
1/1331 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in OTOS 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 18 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 131 mutations in OTOS

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