PLPP3

Phospholipid phosphatase 3 O14495 PLPP3_HUMAN
Protein Coding Chr 1 1p32.2 Swiss-Prot reviewed Entrez 8613
Mutations
182
CL 44 · Tissue 138
Samples
179
CL 44 · Tissue 135
Peptides
123
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
Mutations18244138
Samples17944135
Peptides12328100

Function

PLPP3 · Phospholipid phosphatase 3

The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. This protein is a membrane glycoprotein localized at the cell plasma membrane. It has been shown to actively hydrolyze extracellular lysophosphatidic acid and short-chain phosphatidic acid. The expression of this gene is found to be enhanced by epidermal growth factor in Hela cells. [provided by RefSeq, Mar 2010].

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
ENST00000371250 O14495 182 123

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p32.2
Entrez ID
Aliases
Dri42LPP3PAP2BPPAP2BVCIP

Recurrent Mutations

All 123 amino-acid changes on canonical ENST00000371250 · 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 PLPP3 · 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 PLPP3 – 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
2/40 5%
0/0 0%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
4/210 2%
32/1899 2%
Cervical Carcinoma
0/35 0%
6/422 1%
Endometrial Carcinoma
1/42 2%
5/612 1%
Colorectal Carcinoma
12/143 8%
18/3239 1%
Neuroendocrine Tumour
3/154 2%
3/577 1%
Non-Small Cell Lung Carcinoma
4/304 1%
9/1390 1%
Squamous Cell Lung Carcinoma
3/57 5%
3/810 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Osteosarcoma
0/45 0%
1/166 1%
Thyroid Gland Carcinoma
2/45 4%
5/1592 0%
Meningioma
1/3 33%
0/252 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Kidney Carcinoma
1/85 1%
4/1862 0%
Head and Neck Carcinoma
3/85 4%
1/1574 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Other Blood Cancers
0/61 0%
5/2725 0%
Breast Carcinoma
0/144 0%
6/3264 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Neuroblastoma
0/87 0%
2/1331 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Non-Cancerous
0/104 0%
1/830 0%

Mutation Distribution

Where PLPP3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PLPP3 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 182 mutations in PLPP3

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