CAT

Catalase P04040 CATA_HUMAN
Protein Coding Chr 11 11p13 Swiss-Prot reviewed Entrez 847
Mutations
249
CL 53 · Tissue 186
Samples
234
CL 50 · Tissue 176
Peptides
185
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
Mutations24953186
Samples23450176
Peptides18538148

Function

CAT · Catalase

This gene encodes catalase, a key antioxidant enzyme in the bodies defense against oxidative stress. Catalase is a heme enzyme that is present in the peroxisome of nearly all aerobic cells. Catalase converts the reactive oxygen species hydrogen peroxide to water and oxygen and thereby mitigates the toxic effects of hydrogen peroxide. Oxidative stress is hypothesized to play a role in the development of many chronic or late-onset diseases such as diabetes, asthma, Alzheimer's disease, systemic lupus erythematosus, rheumatoid arthritis, and cancers. Polymorphisms in this gene have been associated with decreases in catalase activity but, to date, acatalasemia is the only disease known to be caused by this gene. [provided by RefSeq, Oct 2009].

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
ENST00000241052 P04040 249 185

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11p13
Entrez ID

Recurrent Mutations

All 185 amino-acid changes on canonical ENST00000241052 · 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 CAT · 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 CAT – 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-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Endometrial Carcinoma
1/42 2%
12/612 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Melanoma
7/210 3%
29/1899 2%
Bladder Carcinoma
2/58 3%
11/956 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Rhabdomyosarcoma
1/33 3%
1/171 1%
Cervical Carcinoma
1/35 3%
3/422 1%
Colorectal Carcinoma
4/143 3%
24/3239 1%
Neuroendocrine Tumour
6/154 4%
0/577 0%
Gastric Carcinoma
0/74 0%
14/1809 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Non-Small Cell Lung Carcinoma
4/304 1%
6/1390 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
14/2550 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Carcinoma
1/23 4%
3/769 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Hepatocellular Carcinoma
0/46 0%
11/2210 0%
Osteosarcoma
0/45 0%
1/166 1%
Medulloblastoma
0/0 0%
2/450 0%
Head and Neck Carcinoma
2/85 2%
5/1574 0%
Glioma
0/52 0%
7/2127 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Other Sarcomas
0/69 0%
2/699 0%
Thyroid Gland Carcinoma
1/45 2%
3/1592 0%
Squamous Cell Lung Carcinoma
1/57 2%
1/810 0%
Breast Carcinoma
4/144 3%
3/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in CAT 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 249 mutations in CAT

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