PEBP4

Phosphatidylethanolamine binding protein 4 Q96S96 PEBP4_HUMAN
Protein Coding Chr 8 8p21.3 Swiss-Prot reviewed Entrez 157310
Mutations
162
CL 50 · Tissue 112
Samples
156
CL 50 · Tissue 106
Peptides
78
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
Mutations16250112
Samples15650106
Peptides781566

Function

PEBP4 · Phosphatidylethanolamine binding protein 4

The phosphatidylethanolamine (PE)-binding proteins, including PEBP4, are an evolutionarily conserved family of proteins with pivotal biologic functions, such as lipid binding and inhibition of serine proteases (Wang et al., 2004 [PubMed 15302887]).[supplied by OMIM, Dec 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
ENST00000256404 Q96S96 162 78

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8p21.3
Entrez ID
Aliases
CORK-1CORK1GWTM1933HEL-S-300PEBP-4PRO4408

Recurrent Mutations

All 78 amino-acid changes on canonical ENST00000256404 · 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 PEBP4 · 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 PEBP4 – 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
3/25 12%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Glioblastoma
3/98 3%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Burkitts Lymphoma
3/32 9%
0/196 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Thyroid Gland Carcinoma
2/45 4%
15/1592 1%
Melanoma
1/210 0%
19/1899 1%
Neuroendocrine Tumour
6/154 4%
0/577 0%
Cervical Carcinoma
0/35 0%
3/422 1%
Colorectal Carcinoma
6/143 4%
16/3239 0%
Non-Cancerous
3/104 3%
3/830 0%
Endometrial Carcinoma
2/42 5%
2/612 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Mesothelioma
1/62 2%
0/165 0%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Prostate Carcinoma
2/13 15%
4/2105 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Glioma
2/52 4%
3/2127 0%
Breast Carcinoma
4/144 3%
4/3264 0%
Neuroblastoma
3/87 3%
0/1331 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Blood Cancers
2/61 3%
1/2725 0%
Ovarian Carcinoma
0/109 0%
1/998 0%

Mutation Distribution

Where PEBP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PEBP4 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 162 mutations in PEBP4

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