CAPN15

Calpain 15 O75808 CAN15_HUMAN
Protein Coding Chr 16 16p13.3 Swiss-Prot reviewed Entrez 6650
Mutations
552
CL 125 · Tissue 416
Samples
502
CL 115 · Tissue 377
Peptides
406
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
Mutations552125416
Samples502115377
Peptides40695316

Function

CAPN15 · Calpain 15

This gene encodes a protein containing zinc-finger-like repeats and a calpain-like protease domain. The encoded protein may function as a transcription factor, RNA-binding protein, or in protein-protein interactions during visual system development. [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
ENST00000219611 O75808 552 406

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.3
Entrez ID
Aliases
OGINSOLH

Recurrent Mutations

All 405 amino-acid changes on canonical ENST00000219611 · 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 CAPN15 · 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 CAPN15 – 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
8/40 20%
0/0 0%
Chronic Myelogenous Leukemia
3/25 12%
0/0 0%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Melanoma
7/210 3%
61/1899 3%
Endometrial Carcinoma
3/42 7%
14/612 2%
Unknown
1/10 10%
0/29 0%
Colorectal Carcinoma
8/143 6%
70/3239 2%
Glioblastoma
2/98 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Thyroid Gland Carcinoma
2/45 4%
26/1592 2%
Gastric Carcinoma
3/74 4%
29/1809 2%
Neuroendocrine Tumour
5/154 3%
7/577 1%
Non-Small Cell Lung Carcinoma
10/304 3%
15/1390 1%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Squamous Cell Lung Carcinoma
3/57 5%
9/810 1%
Burkitts Lymphoma
0/32 0%
3/196 2%
Other Solid Cancers
2/94 2%
16/1515 1%
Cervical Carcinoma
4/35 11%
1/422 0%
Non-Cancerous
1/104 1%
9/830 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Bladder Carcinoma
0/58 0%
10/956 1%
Other Sarcomas
2/69 3%
5/699 1%
Ovarian Carcinoma
6/109 6%
4/998 0%
Mesothelioma
2/62 3%
0/165 0%
Head and Neck Carcinoma
0/85 0%
13/1574 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Neuroblastoma
9/87 10%
1/1331 0%
Hepatocellular Carcinoma
2/46 4%
14/2210 1%
Biliary Tract Carcinoma
1/54 2%
6/950 1%

Mutation Distribution

Where CAPN15 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CAPN15 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 54 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 552 mutations in CAPN15

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