STON1

Stonin 1 Q9Y6Q2 STON1_HUMAN
Protein Coding Chr 2 2p16.3 Swiss-Prot reviewed Entrez 11037
Mutations
966
CL 120 · Tissue 832
Samples
458
CL 78 · Tissue 371
Peptides
336
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
Mutations966120832
Samples45878371
Peptides33644292

Function

STON1 · Stonin 1

Endocytosis of cell surface proteins is mediated by a complex molecular machinery that assembles on the inner surface of the plasma membrane. This gene encodes one of two human homologs of the Drosophila melanogaster stoned B protein. This protein is related to components of the endocytic machinery and exhibits a modular structure consisting of an N-terminal proline-rich domain, a central region of homology specific to the human stoned B-like proteins, and a C-terminal region homologous to the mu subunits of adaptor protein (AP) complexes. Read-through transcription of this gene into the neighboring downstream gene, which encodes TFIIA-alpha/beta-like factor, generates a transcript (SALF), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010].

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
ENST00000404752 Q9Y6Q2 505 336
ENST00000406226 Q9Y6Q2 461 323

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p16.3
Entrez ID
Aliases
SALFSBLFSTNB1

Recurrent Mutations

All 336 amino-acid changes on canonical ENST00000404752 · 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 STON1 · 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 STON1 – 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%
Melanoma
7/210 3%
76/1899 4%
Endometrial Carcinoma
4/42 10%
17/612 3%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Squamous Cell Lung Carcinoma
3/57 5%
19/810 2%
Non-Small Cell Lung Carcinoma
14/304 5%
29/1390 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Colorectal Carcinoma
11/143 8%
52/3239 2%
Bladder Carcinoma
0/58 0%
18/956 2%
Neuroendocrine Tumour
9/154 6%
3/577 1%
Other Solid Cancers
1/94 1%
20/1515 1%
Gastric Carcinoma
0/74 0%
21/1809 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Germ Cell Tumour
0/25 0%
2/169 1%
Esophageal Carcinoma
0/23 0%
7/769 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Other Sarcomas
0/69 0%
6/699 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
16/2550 1%
Glioma
3/52 6%
10/2127 0%
Pancreatic Carcinoma
0/89 0%
10/1611 1%
Head and Neck Carcinoma
0/85 0%
9/1574 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Breast Carcinoma
5/144 3%
11/3264 0%
Mesothelioma
0/62 0%
1/165 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Kidney Carcinoma
2/85 2%
6/1862 0%
Neuroblastoma
1/87 1%
4/1331 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
4/2534 0%
Hepatocellular Carcinoma
1/46 2%
6/2210 0%

Mutation Distribution

Where STON1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in STON1 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 966 mutations in STON1

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