PPP6R3

Protein phosphatase 6 regulatory subunit 3 Q5H9R7 PP6R3_HUMAN
Protein Coding Chr 11 11q13.2 Swiss-Prot reviewed Entrez 55291
Mutations
2,949
CL 242 · Tissue 2,630
Samples
355
CL 51 · Tissue 295
Peptides
333
unique mutant peptides
Transcripts
9
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
Mutations2,9492422,630
Samples35551295
Peptides33344286

Function

PPP6R3 · Protein phosphatase 6 regulatory subunit 3

Protein phosphatase regulatory subunits, such as SAPS3, modulate the activity of protein phosphatase catalytic subunits by restricting substrate specificity, recruiting substrates, and determining the intracellular localization of the holoenzyme. SAPS3 is a regulatory subunit for the protein phosphatase-6 catalytic subunit (PPP6C; MIM 612725) (Stefansson and Brautigan, 2006 [PubMed 16769727]).[supplied by OMIM, Nov 2010].

Isoforms & Proteins

9 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
ENST00000393800 Q5H9R7 380 285
ENST00000393801 Q5H9R7-5 342 266
ENST00000524845 Q5H9R7-6 337 262
ENST00000524904 Q5H9R7-2 336 260
ENST00000527403 E9PKF6* 332 257
ENST00000265637 H7BXH2* 328 254
ENST00000265636 Q5H9R7-4 324 253
ENST00000529710 Q5H9R7-3 321 250
ENST00000534534 E9PQP7* 249 191

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.2
Entrez ID
Aliases
C11orf23PP6R3SAP190SAPLSAPLaSAPS3

Recurrent Mutations

All 285 amino-acid changes on canonical ENST00000393800 · 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 PPP6R3 · 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 PPP6R3 – 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
5/40 12%
0/0 0%
Endometrial Carcinoma
1/42 2%
25/612 4%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
5/210 2%
37/1899 2%
Meningioma
1/3 33%
4/252 2%
Colorectal Carcinoma
7/143 5%
42/3239 1%
Squamous Cell Lung Carcinoma
2/57 4%
10/810 1%
Ovarian Carcinoma
7/109 6%
6/998 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Head and Neck Carcinoma
1/85 1%
17/1574 1%
Non-Cancerous
1/104 1%
9/830 1%
Non-Small Cell Lung Carcinoma
4/304 1%
12/1390 1%
Hepatocellular Carcinoma
0/46 0%
21/2210 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
23/2550 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Gastric Carcinoma
3/74 4%
11/1809 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Other Solid Cancers
0/94 0%
8/1515 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Osteosarcoma
0/45 0%
1/166 1%
Prostate Carcinoma
0/13 0%
10/2105 0%
Breast Carcinoma
1/144 1%
13/3264 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Other Sarcomas
1/69 1%
2/699 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
8/2534 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%

Mutation Distribution

Where PPP6R3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PPP6R3 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 2,949 mutations in PPP6R3

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