STATH

Statherin P02808 STAT_HUMAN
Protein Coding Chr 4 4q13.3 Swiss-Prot reviewed Entrez 6779
Mutations
80
CL 14 · Tissue 66
Samples
46
CL 10 · Tissue 36
Peptides
46
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
Mutations801466
Samples461036
Peptides46938

Function

STATH · Statherin

Predicted to be involved in ossification. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000246895 P02808 46 33
ENST00000381060 P02808-2 34 25

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q13.3
Entrez ID
Aliases
STR

Recurrent Mutations

All 33 amino-acid changes on canonical ENST00000246895 · 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 STATH · 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 STATH – 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
Endometrial Carcinoma
1/42 2%
3/612 0%
Melanoma
0/210 0%
9/1899 0%
Non-Cancerous
0/104 0%
3/830 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Non-Small Cell Lung Carcinoma
0/304 0%
4/1390 0%
Breast Carcinoma
2/144 1%
4/3264 0%
Gastric Carcinoma
1/74 1%
2/1809 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Glioma
0/52 0%
2/2127 0%
Colorectal Carcinoma
2/143 1%
0/3239 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in STATH 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 4 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 80 mutations in STATH

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