OTOL1

Otolin 1 A6NHN0 OTOL1_HUMAN
Protein Coding Chr 3 3q26.1 Swiss-Prot reviewed Entrez 131149
Mutations
567
CL 124 · Tissue 441
Samples
508
CL 115 · Tissue 391
Peptides
340
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
Mutations567124441
Samples508115391
Peptides34077285

Function

OTOL1 · Otolin 1

This gene encodes a secreted glycoprotein with a C-terminal complement Cq1-like globular domain that belongs to the C1q/tumor necrosis factor-related protein (CTRP) family. The encoded protein is expressed in the inner ear and forms a multimeric complex called the otoconia, together with cerebellin-1 and otoconin-90, as part of the otoconial membrane. It contains extensive posttranslational modifications including hydroxylated prolines and glycosylated lysines. Naturally occurring mutations in this gene are associated with abnormal otoconia formation and balance deficits resulting from vestibular dysfunction. [provided by RefSeq, Jul 2017].

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
ENST00000327928 A6NHN0 567 340

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q26.1
Entrez ID
Aliases
C1QTNF15C1QTNF16

Recurrent Mutations

All 340 amino-acid changes on canonical ENST00000327928 · 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 OTOL1 · 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 OTOL1 – 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
Glioblastoma
6/98 6%
0/0 0%
Melanoma
19/210 9%
100/1899 5%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Other Solid Cancers
4/94 4%
44/1515 3%
Non-Small Cell Lung Carcinoma
26/304 9%
24/1390 2%
Squamous Cell Lung Carcinoma
5/57 9%
17/810 2%
Endometrial Carcinoma
1/42 2%
14/612 2%
Colorectal Carcinoma
13/143 9%
30/3239 1%
Esophageal Carcinoma
0/23 0%
10/769 1%
Esophageal Squamous Cell Carcinoma
4/51 8%
28/2550 1%
Neuroendocrine Tumour
5/154 3%
3/577 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Other Sarcomas
2/69 3%
5/699 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Mesothelioma
2/62 3%
0/165 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Gastric Carcinoma
4/74 5%
11/1809 1%
Thyroid Gland Carcinoma
0/45 0%
12/1592 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Cervical Carcinoma
1/35 3%
2/422 0%
Ewings Sarcoma
2/63 3%
0/262 0%
Bladder Carcinoma
1/58 2%
5/956 1%
Hepatocellular Carcinoma
2/46 4%
11/2210 0%
Ovarian Carcinoma
0/109 0%
6/998 1%
Non-Cancerous
1/104 1%
4/830 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Head and Neck Carcinoma
3/85 4%
5/1574 0%
Osteosarcoma
1/45 2%
0/166 0%

Mutation Distribution

Where OTOL1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in OTOL1 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 4 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 567 mutations in OTOL1

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