MPPE1

Metallophosphoesterase 1 Q53F39 MPPE1_HUMAN
Protein Coding Chr 18 18p11.21 Swiss-Prot reviewed Entrez 65258
Mutations
441
CL 53 · Tissue 382
Samples
139
CL 17 · Tissue 117
Peptides
125
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
Mutations44153382
Samples13917117
Peptides12516110

Function

MPPE1 · Metallophosphoesterase 1

Predicted to enable GPI anchor binding activity; GPI-mannose ethanolamine phosphate phosphodiesterase activity; and manganese ion binding activity. Involved in GPI anchor biosynthetic process. Located in Golgi apparatus and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000588072 Q53F39 144 109
ENST00000344987 A0A0A0MR93* 123 95
ENST00000309976 Q53F39-4 87 76
ENST00000317235 Q53F39-4 87 76

Gene Properties

Type
Protein Coding
Chromosome
18
Cytoband
18p11.21
Entrez ID
Aliases
Cdc1PGAP5

Recurrent Mutations

All 109 amino-acid changes on canonical ENST00000588072 · 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 MPPE1 · 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 MPPE1 – 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%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Endometrial Carcinoma
0/42 0%
11/612 2%
Melanoma
0/210 0%
22/1899 1%
Non-Small Cell Lung Carcinoma
9/304 3%
7/1390 0%
Gastric Carcinoma
2/74 3%
11/1809 1%
Colorectal Carcinoma
0/143 0%
20/3239 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Other Solid Cancers
0/94 0%
7/1515 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Non-Cancerous
0/104 0%
2/830 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Glioma
0/52 0%
4/2127 0%
Other Sarcomas
0/69 0%
1/699 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Neuroblastoma
1/87 1%
0/1331 0%
Breast Carcinoma
0/144 0%
2/3264 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%

Mutation Distribution

Where MPPE1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MPPE1 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 441 mutations in MPPE1

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