PAGE4

PAGE family member 4 O60829 PAGE4_HUMAN
Protein Coding Chr X Xp11.23 Swiss-Prot reviewed Entrez 9506
Mutations
79
CL 17 · Tissue 62
Samples
41
CL 12 · Tissue 29
Peptides
34
unique mutant peptides
Transcripts
2
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
Mutations791762
Samples411229
Peptides34828

Function

PAGE4 · PAGE family member 4

This gene is a member of the GAGE family. The GAGE genes are expressed in a variety of tumors and in some fetal and reproductive tissues. This gene is strongly expressed in prostate and prostate cancer. It is also expressed in other male and female reproductive tissues including testis, fallopian tube, uterus, and placenta, as well as in testicular cancer and uterine cancer. The protein encoded by this gene shares sequence similarity with other GAGE/PAGE proteins, and also belongs to a family of CT (cancer-testis) antigens. The protein may play a role in benign and malignant prostate diseases. A related pseudogene is located on chromosome 7. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016].

Isoforms & Proteins

2 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
ENST00000218068 O60829 43 34
ENST00000376141 O60829 36 31

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp11.23
Entrez ID
Aliases
CT16.7GAGE-9GAGEC1JM-27JM27PAGE-1

Recurrent Mutations

All 34 amino-acid changes on canonical ENST00000218068 · 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 PAGE4 · 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 PAGE4 – 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
Glioblastoma
1/98 1%
0/0 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Endometrial Carcinoma
1/42 2%
3/612 0%
Melanoma
2/210 1%
9/1899 0%
Ovarian Carcinoma
3/109 3%
0/998 0%
Non-Small Cell Lung Carcinoma
0/304 0%
4/1390 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Gastric Carcinoma
2/74 3%
1/1809 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Colorectal Carcinoma
2/143 1%
2/3239 0%
Glioma
0/52 0%
2/2127 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
Other Blood Cancers
1/61 2%
0/2725 0%

Mutation Distribution

Where PAGE4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PAGE4 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 22 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 79 mutations in PAGE4

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