PDPR

Pyruvate dehydrogenase phosphatase regulatory subunit Q8NCN5 PDPR_HUMAN
Protein Coding Chr 16 16q22.1 Swiss-Prot reviewed Entrez 55066
Mutations
1,851
CL 372 · Tissue 1,457
Samples
508
CL 111 · Tissue 390
Peptides
348
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
Mutations1,8513721,457
Samples508111390
Peptides34880274

Function

PDPR · Pyruvate dehydrogenase phosphatase regulatory subunit

Pyruvate dehydrogenase complex (PDC) catalyzes the oxidative decarboxylation of pyruvate and links glycolysis to the tricarboxylic acid cycle and fatty acid synthesis. The dephosphorylation and reactivation of PDC is catalyzed by pyruvate dehydrogenase phosphatase (PDP). The dimeric PDP has a catalytic subunit and a regulatory subunit. This gene encodes the FAD-containing regulatory subunit of PDP. The encoded protein acts to decrease the sensitivity of the PDP catalytic subunit to magnesium ions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017].

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
ENST00000288050 Q8NCN5 600 339
ENST00000568530 Q8NCN5 578 326
ENST00000398122 A8MT40* 516 293
ENST00000567046 B7ZAR9* 157 97

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16q22.1
Entrez ID
Aliases
PDP3

Recurrent Mutations

All 338 amino-acid changes on canonical ENST00000288050 · 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 PDPR · 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 PDPR – 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
4/40 10%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
7/42 17%
26/612 4%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Non-Small Cell Lung Carcinoma
29/304 10%
24/1390 2%
Melanoma
6/210 3%
41/1899 2%
Squamous Cell Lung Carcinoma
7/57 12%
11/810 1%
Glioblastoma
2/98 2%
0/0 0%
Colorectal Carcinoma
10/143 7%
59/3239 2%
Gastric Carcinoma
8/74 11%
28/1809 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Other Solid Cancers
1/94 1%
23/1515 2%
Neuroendocrine Tumour
7/154 5%
3/577 1%
Chondrosarcoma
1/14 7%
0/75 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Thyroid Gland Carcinoma
1/45 2%
17/1592 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Bladder Carcinoma
1/58 2%
10/956 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Hepatocellular Carcinoma
1/46 2%
18/2210 1%
Ovarian Carcinoma
1/109 1%
8/998 1%
Other Sarcomas
0/69 0%
6/699 1%
Non-Cancerous
1/104 1%
6/830 1%
Head and Neck Carcinoma
0/85 0%
11/1574 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Prostate Carcinoma
1/13 8%
12/2105 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
15/2550 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Glioma
2/52 4%
9/2127 0%
Osteosarcoma
1/45 2%
0/166 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in PDPR 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 1,851 mutations in PDPR

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