PGAP6

Post-GPI attachment to proteins 6 Q9HCN3 PGAP6_HUMAN
Protein Coding Chr 16 16p13.3 Swiss-Prot reviewed Entrez 58986
Mutations
67
CL 50 · Tissue 0
Samples
51
CL 43 · Tissue 0
Peptides
62
unique mutant peptides
Transcripts
1
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
Mutations67500
Samples51430
Peptides62450

Function

PGAP6 · Post-GPI attachment to proteins 6

Predicted to enable phospholipase A2 activity. Located in extracellular exosome and lysosomal membrane. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

1 transcript · 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
ENST00000431232 Q9HCN3 67 62

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.3
Entrez ID
Aliases
GPI-PLA2M83TMEM6TMEM8TMEM8A

Recurrent Mutations

All 62 amino-acid changes on canonical ENST00000431232 · 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 PGAP6 · 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 PGAP6 – 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
4/40 10%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Burkitts Lymphoma
2/32 6%
0/196 0%
Endometrial Carcinoma
4/42 10%
1/612 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Ovarian Carcinoma
3/109 3%
0/998 0%
Gastric Carcinoma
3/74 4%
1/1809 0%
Melanoma
3/210 1%
1/1899 0%
Colorectal Carcinoma
4/143 3%
2/3239 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Non-Small Cell Lung Carcinoma
2/304 1%
1/1390 0%
Other Sarcomas
1/69 1%
0/699 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Non-Cancerous
1/104 1%
0/830 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
0/2534 0%
Hepatocellular Carcinoma
2/46 4%
0/2210 0%
Other Blood Cancers
2/61 3%
0/2725 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
0/2550 0%

Mutation Distribution

Where PGAP6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PGAP6 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.

Mutations

All 67 mutations in PGAP6

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