TNS3

Tensin 3 Q68CZ2 TENS3_HUMAN
Protein Coding Chr 7 7p12.3 Swiss-Prot reviewed Entrez 64759
Mutations
974
CL 177 · Tissue 783
Samples
769
CL 142 · Tissue 616
Peptides
619
unique mutant peptides
Transcripts
3
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
Mutations974177783
Samples769142616
Peptides619103533

Function

TNS3 · Tensin 3

Predicted to enable phosphatase activity. Predicted to be involved in dephosphorylation and intracellular signal transduction. Predicted to act upstream of or within cell migration; lung alveolus development; and positive regulation of cell population proliferation. Located in cytosol and focal adhesion. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

3 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
ENST00000311160 Q68CZ2 854 611
ENST00000442536 Q68CZ2-4 117 95
ENST00000705350 A0A994J537* 3 3

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p12.3
Entrez ID
Aliases
TEM6TENS1

Recurrent Mutations

All 611 amino-acid changes on canonical ENST00000311160 · 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 TNS3 · 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 TNS3 – 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
6/40 15%
0/0 0%
Chordoma
2/7 29%
1/13 8%
Endometrial Carcinoma
4/42 10%
40/612 7%
Melanoma
13/210 6%
84/1899 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Colorectal Carcinoma
19/143 13%
90/3239 3%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Gastric Carcinoma
5/74 7%
51/1809 3%
Non-Small Cell Lung Carcinoma
16/304 5%
29/1390 2%
Bladder Carcinoma
2/58 3%
25/956 3%
Burkitts Lymphoma
0/32 0%
6/196 3%
Other Solid Cancers
0/94 0%
39/1515 3%
Cervical Carcinoma
2/35 6%
9/422 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Neuroendocrine Tumour
11/154 7%
4/577 1%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Squamous Cell Lung Carcinoma
6/57 11%
10/810 1%
Ovarian Carcinoma
9/109 8%
10/998 1%
Non-Cancerous
1/104 1%
14/830 2%
Small Cell Lung Carcinoma
0/9 0%
12/752 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
33/2550 1%
Ewings Sarcoma
4/63 6%
0/262 0%
Head and Neck Carcinoma
2/85 2%
18/1574 1%
Hepatocellular Carcinoma
3/46 7%
21/2210 1%
Glioblastoma
1/98 1%
0/0 0%
Thyroid Gland Carcinoma
3/45 7%
13/1592 1%
Glioma
1/52 2%
20/2127 1%
Osteosarcoma
2/45 4%
0/166 0%

Mutation Distribution

Where TNS3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TNS3 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 974 mutations in TNS3

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