PSMA4

Proteasome 20S subunit alpha 4 P25789 PSA4_HUMAN
Protein Coding Chr 15 15q25.1 Swiss-Prot reviewed Entrez 5685
Mutations
401
CL 48 · Tissue 348
Samples
91
CL 20 · Tissue 69
Peptides
99
unique mutant peptides
Transcripts
7
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
Mutations40148348
Samples912069
Peptides991684

Function

PSMA4 · Proteasome 20S subunit alpha 4

This gene encodes a core alpha subunit of the 20S proteosome, which is a highly ordered ring-shaped structure composed of four rings of 28 non-identical subunits. Proteasomes cleave peptides in an ATP- and ubiquitin-dependent manner. [provided by RefSeq, Aug 2016].

Isoforms & Proteins

7 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
ENST00000044462 P25789 88 70
ENST00000559082 P25789 75 63
ENST00000560217 H0YN18* 72 60
ENST00000413382 P25789-2 54 45
ENST00000558281 H0YLC2* 52 45
ENST00000558341 H0YLS6* 33 30
ENST00000558094 H0YMV3* 27 23

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q25.1
Entrez ID
Aliases
HC9HsT17706PSC9

Recurrent Mutations

All 70 amino-acid changes on canonical ENST00000044462 · 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 PSMA4 · 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 PSMA4 – 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-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Endometrial Carcinoma
0/42 0%
6/612 1%
Melanoma
4/210 2%
10/1899 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Osteosarcoma
1/45 2%
0/166 0%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Hepatocellular Carcinoma
2/46 4%
7/2210 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Colorectal Carcinoma
1/143 1%
9/3239 0%
Gastric Carcinoma
2/74 3%
3/1809 0%
Medulloblastoma
0/0 0%
1/450 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Glioma
0/52 0%
2/2127 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Thyroid Gland Carcinoma
0/45 0%
1/1592 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where PSMA4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PSMA4 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 401 mutations in PSMA4

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