MPP4

MAGUK p55 scaffold protein 4 Q96JB8 MPP4_HUMAN
Protein Coding Chr 2 2q33.1 Swiss-Prot reviewed Entrez 58538
Mutations
2,506
CL 295 · Tissue 2,175
Samples
328
CL 60 · Tissue 262
Peptides
305
unique mutant peptides
Transcripts
8
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
Mutations2,5062952,175
Samples32860262
Peptides30545259

Function

MPP4 · MAGUK p55 scaffold protein 4

This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) protein family, with an N-terminal PDZ domain, a central src homology 3 region (SH3), and a C-terminal guanylate kinase-like (GUK) domain. The protein is localized to the outer limiting membrane in the retina, and is thought to function in photoreceptor polarity and the organization of specialized intercellular junctions. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

8 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
ENST00000409474 Q96JB8 349 257
ENST00000359962 E7EUL8* 320 245
ENST00000447335 E7EUL8* 320 245
ENST00000428900 E7ET46* 313 242
ENST00000620095 A0A087WUS1* 310 240
ENST00000315506 Q96JB8-2 306 235
ENST00000409143 F6Q0Y6* 295 229
ENST00000396886 E9PG92* 293 223

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q33.1
Entrez ID
Aliases
ALS2CR5DLG6

Recurrent Mutations

All 257 amino-acid changes on canonical ENST00000409474 · 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 MPP4 · 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 MPP4 – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
4/42 10%
16/612 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Retinoblastoma
1/27 4%
0/30 0%
Colorectal Carcinoma
18/143 13%
40/3239 1%
Melanoma
5/210 2%
28/1899 1%
Squamous Cell Lung Carcinoma
2/57 4%
11/810 1%
Biliary Tract Carcinoma
0/54 0%
12/950 1%
Gastric Carcinoma
3/74 4%
17/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Non-Small Cell Lung Carcinoma
5/304 2%
12/1390 1%
Osteosarcoma
1/45 2%
1/166 1%
Mesothelioma
1/62 2%
1/165 1%
Other Solid Cancers
0/94 0%
14/1515 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
19/2550 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Other Sarcomas
0/69 0%
5/699 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Ovarian Carcinoma
1/109 1%
5/998 0%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Esophageal Carcinoma
0/23 0%
4/769 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Glioma
1/52 2%
9/2127 0%
Medulloblastoma
0/0 0%
2/450 0%
Meningioma
0/3 0%
1/252 0%
Bladder Carcinoma
1/58 2%
3/956 0%
Breast Carcinoma
2/144 1%
10/3264 0%

Mutation Distribution

Where MPP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MPP4 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 53 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 2,506 mutations in MPP4

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