CASP4

Caspase 4 P49662 CASP4_HUMAN
Protein Coding Chr 11 11q22.3 Swiss-Prot reviewed Entrez 837
Mutations
325
CL 55 · Tissue 266
Samples
186
CL 39 · Tissue 143
Peptides
145
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
Mutations32555266
Samples18639143
Peptides14525120

Function

CASP4 · Caspase 4

This gene encodes a protein that is a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain and a large and small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This caspase is able to cleave and activate its own precursor protein, as well as caspase 1 precursor. When overexpressed, this gene induces cell apoptosis. Alternative splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 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
ENST00000444739 P49662 190 143
ENST00000393150 P49662-2 135 110

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q22.3
Entrez ID
Aliases
CASP-4ICE(rel)IIICEREL-IIICH-2Mih1Mih1/TX

Recurrent Mutations

All 143 amino-acid changes on canonical ENST00000444739 · 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 CASP4 · 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 CASP4 – 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
Chronic Myelogenous Leukemia
4/25 16%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Endometrial Carcinoma
3/42 7%
8/612 1%
Non-Small Cell Lung Carcinoma
6/304 2%
12/1390 1%
Gastric Carcinoma
1/74 1%
18/1809 1%
Squamous Cell Lung Carcinoma
0/57 0%
8/810 1%
Hepatocellular Carcinoma
4/46 9%
14/2210 1%
Colorectal Carcinoma
2/143 1%
21/3239 1%
Melanoma
0/210 0%
14/1899 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Bladder Carcinoma
1/58 2%
4/956 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Mesothelioma
1/62 2%
0/165 0%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
7/2550 0%
Other Sarcomas
0/69 0%
2/699 0%
Pancreatic Carcinoma
1/89 1%
3/1611 0%
Glioma
0/52 0%
5/2127 0%
Non-Cancerous
0/104 0%
2/830 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Neuroblastoma
2/87 2%
0/1331 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Prostate Carcinoma
2/13 15%
0/2105 0%
Breast Carcinoma
0/144 0%
3/3264 0%

Mutation Distribution

Where CASP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CASP4 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 325 mutations in CASP4

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