MPI

Mannose phosphate isomerase P34949 MPI_HUMAN
Protein Coding Chr 15 15q24.1-q24.2 Swiss-Prot reviewed Entrez 4351
Mutations
813
CL 116 · Tissue 691
Samples
149
CL 29 · Tissue 116
Peptides
138
unique mutant peptides
Transcripts
9
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
Mutations813116691
Samples14929116
Peptides13825109

Function

MPI · Mannose phosphate isomerase

Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014].

Isoforms & Proteins

9 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
ENST00000352410 P34949 141 110
ENST00000563786 H3BPB8* 119 98
ENST00000535694 F5GX71* 111 90
ENST00000323744 P34949-2 109 88
ENST00000563422 H3BUZ9* 76 70
ENST00000562606 H3BT48* 73 67
ENST00000566377 H3BPP3* 71 65
ENST00000565576 H3BMZ9* 59 49
ENST00000564003 B4DYB8* 54 48

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q24.1-q24.2
Entrez ID
Aliases
CDG1BPMIPMI1

Recurrent Mutations

All 110 amino-acid changes on canonical ENST00000352410 · 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 MPI · 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 MPI – 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
5/40 12%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Endometrial Carcinoma
1/42 2%
9/612 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Melanoma
2/210 1%
15/1899 1%
Non-Small Cell Lung Carcinoma
3/304 1%
10/1390 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Colorectal Carcinoma
6/143 4%
15/3239 0%
Bladder Carcinoma
0/58 0%
6/956 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Other Solid Cancers
0/94 0%
7/1515 0%
Squamous Cell Lung Carcinoma
1/57 2%
2/810 0%
Hepatocellular Carcinoma
1/46 2%
7/2210 0%
Non-Cancerous
0/104 0%
3/830 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Breast Carcinoma
1/144 1%
9/3264 0%
Thyroid Gland Carcinoma
1/45 2%
3/1592 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Prostate Carcinoma
2/13 15%
1/2105 0%
Glioma
0/52 0%
3/2127 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MPI 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 813 mutations in MPI

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