PKP3

Plakophilin 3 Q9Y446 PKP3_HUMAN
Protein Coding Chr 11 11p15.5 Swiss-Prot reviewed Entrez 11187
Mutations
379
CL 79 · Tissue 290
Samples
350
CL 71 · Tissue 270
Peptides
263
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
Mutations37979290
Samples35071270
Peptides26354215

Function

PKP3 · Plakophilin 3

This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may act in cellular desmosome-dependent adhesion and signaling pathways. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014].

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
ENST00000331563 Q9Y446 379 263

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11p15.5
Entrez ID

Recurrent Mutations

All 263 amino-acid changes on canonical ENST00000331563 · 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 PKP3 · 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 PKP3 – 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%
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Endometrial Carcinoma
7/42 17%
12/612 2%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
6/210 3%
32/1899 2%
Esophageal Carcinoma
2/23 9%
10/769 1%
Thyroid Gland Carcinoma
1/45 2%
21/1592 1%
Burkitts Lymphoma
1/32 3%
2/196 1%
Cervical Carcinoma
0/35 0%
6/422 1%
Other Solid Cancers
3/94 3%
18/1515 1%
Colorectal Carcinoma
5/143 4%
38/3239 1%
Gastric Carcinoma
4/74 5%
20/1809 1%
Chondrosarcoma
1/14 7%
0/75 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Biliary Tract Carcinoma
0/54 0%
11/950 1%
Non-Cancerous
1/104 1%
8/830 1%
Squamous Cell Lung Carcinoma
2/57 4%
6/810 1%
Other Sarcomas
0/69 0%
7/699 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Esophageal Squamous Cell Carcinoma
4/51 8%
15/2550 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Glioma
0/52 0%
12/2127 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Mesothelioma
1/62 2%
0/165 0%
Hepatocellular Carcinoma
0/46 0%
10/2210 0%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Meningioma
1/3 33%
0/252 0%

Mutation Distribution

Where PKP3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PKP3 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 379 mutations in PKP3

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