CASP10

Caspase 10 Q92851 CASPA_HUMAN
Protein Coding Chr 2 2q33.1 Swiss-Prot reviewed Entrez 843
Mutations
1,079
CL 148 · Tissue 911
Samples
238
CL 45 · Tissue 188
Peptides
213
unique mutant peptides
Transcripts
7
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
Mutations1,079148911
Samples23845188
Peptides21334179

Function

CASP10 · Caspase 10

This gene encodes a protein which 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 which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein cleaves and activates caspases 3 and 7, and the protein itself is processed by caspase 8. Mutations in this gene are associated with type IIA autoimmune lymphoproliferative syndrome, non-Hodgkin lymphoma and gastric cancer. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011].

Isoforms & Proteins

7 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
ENST00000286186 Q92851-4 226 163
ENST00000272879 Q92851 194 149
ENST00000346817 Q92851-2 190 141
ENST00000313728 Q92851-6 187 137
ENST00000448480 Q92851-5 179 138
ENST00000374650 Q92851-7 94 66
ENST00000492363 Q92851-3 9 8

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q33.1
Entrez ID
Aliases
ALPS2FLICE-2FLICE2MCH4

Recurrent Mutations

All 163 amino-acid changes on canonical ENST00000286186 · 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 CASP10 · 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 CASP10 – 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
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Rhabdomyosarcoma
1/33 3%
4/171 2%
Endometrial Carcinoma
4/42 10%
11/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Melanoma
3/210 1%
40/1899 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Colorectal Carcinoma
13/143 9%
25/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Osteosarcoma
2/45 4%
0/166 0%
Non-Small Cell Lung Carcinoma
5/304 2%
11/1390 1%
Gastric Carcinoma
0/74 0%
17/1809 1%
Mesothelioma
2/62 3%
0/165 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Other Sarcomas
0/69 0%
3/699 0%
Meningioma
0/3 0%
1/252 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Glioma
0/52 0%
8/2127 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Non-Cancerous
1/104 1%
2/830 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Breast Carcinoma
1/144 1%
7/3264 0%

Mutation Distribution

Where CASP10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CASP10 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 1,079 mutations in CASP10

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