UCP2

Uncoupling protein 2 P55851 UCP2_HUMAN
Protein Coding Chr 11 11q13.4 Swiss-Prot reviewed Entrez 7351
Mutations
356
CL 70 · Tissue 278
Samples
200
CL 43 · Tissue 151
Peptides
120
unique mutant peptides
Transcripts
4
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
Mutations35670278
Samples20043151
Peptides1203197

Function

UCP2 · Uncoupling protein 2

Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. This gene is expressed in many tissues, with the greatest expression in skeletal muscle. It is thought to play a role in nonshivering thermogenesis, obesity and diabetes. Chromosomal order is 5'-UCP3-UCP2-3'. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

4 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
ENST00000310473 P55851 181 103
ENST00000536983 F5GX45* 152 82
ENST00000663595 P55851 22 19
ENST00000545212 H0YFQ0* 1 1

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.4
Entrez ID
Aliases
BMIQ4SLC25A8UCPH

Recurrent Mutations

All 103 amino-acid changes on canonical ENST00000310473 · 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 UCP2 · 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 UCP2 – 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
6/40 15%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Pancreatic Carcinoma
0/89 0%
29/1611 2%
Endometrial Carcinoma
4/42 10%
7/612 1%
Melanoma
3/210 1%
22/1899 1%
Plasma Cell Myeloma
4/44 9%
0/305 0%
Osteosarcoma
2/45 4%
0/166 0%
Colorectal Carcinoma
3/143 2%
25/3239 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Solid Cancers
1/94 1%
9/1515 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Mesothelioma
1/62 2%
0/165 0%
Gastric Carcinoma
1/74 1%
7/1809 0%
Small Cell Lung Carcinoma
2/9 22%
1/752 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Breast Carcinoma
4/144 3%
7/3264 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Non-Cancerous
0/104 0%
2/830 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Prostate Carcinoma
4/13 31%
0/2105 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Non-Small Cell Lung Carcinoma
0/304 0%
3/1390 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
B-Lymphoblastic Leukemia
0/55 0%
3/2640 0%
Glioma
0/52 0%
2/2127 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
1/2550 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%

Mutation Distribution

Where UCP2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in UCP2 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 356 mutations in UCP2

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