PAGE3

PAGE family member 3 Q5JUK9 PAGE3_HUMAN
Protein Coding Chr X Xp11.21 Swiss-Prot reviewed Entrez 139793
Mutations
155
CL 13 · Tissue 142
Samples
78
CL 8 · Tissue 70
Peptides
62
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
Mutations15513142
Samples78870
Peptides62657

Function

PAGE3 · PAGE family member 3

This gene is a member of family of proteins that are expressed in a variety of tumors and in some fetal and reproductive tissues. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2015].

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
ENST00000374951 Q5JUK9 79 62
ENST00000519203 Q5JUK9 76 61

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp11.21
Entrez ID
Aliases
CT16.6GAGED1PAGE-3

Recurrent Mutations

All 62 amino-acid changes on canonical ENST00000374951 · 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 PAGE3 · 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 PAGE3 – 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%
Endometrial Carcinoma
1/42 2%
8/612 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Melanoma
0/210 0%
14/1899 1%
Other Solid Cancers
2/94 2%
5/1515 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Colorectal Carcinoma
1/143 1%
6/3239 0%
Breast Carcinoma
2/144 1%
4/3264 0%
Non-Small Cell Lung Carcinoma
1/304 0%
2/1390 0%
Other Sarcomas
0/69 0%
1/699 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Non-Cancerous
0/104 0%
1/830 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Neuroblastoma
0/87 0%
1/1331 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where PAGE3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PAGE3 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 1 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 155 mutations in PAGE3

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