TEC

Tec protein tyrosine kinase P42680 TEC_HUMAN
Protein Coding Chr 4 4p12-p11 Swiss-Prot reviewed Entrez 7006
Mutations
297
CL 54 · Tissue 240
Samples
288
CL 54 · Tissue 231
Peptides
225
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
Mutations29754240
Samples28854231
Peptides22529196

Function

TEC · Tec protein tyrosine kinase

The protein encoded by this gene belongs to the Tec family of non-receptor protein-tyrosine kinases containing a pleckstrin homology domain. Tec family kinases are involved in the intracellular signaling mechanisms of cytokine receptors, lymphocyte surface antigens, heterotrimeric G-protein coupled receptors, and integrin molecules. They are also key players in the regulation of the immune functions. Tec kinase is an integral component of T cell signaling and has a distinct role in T cell activation. This gene may be associated with myelodysplastic syndrome. [provided by RefSeq, Jul 2008].

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
ENST00000381501 P42680 297 225

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4p12-p11
Entrez ID
Aliases
PSCTK4

Recurrent Mutations

All 225 amino-acid changes on canonical ENST00000381501 · 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 TEC · 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 TEC – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Hodgkins Lymphoma
4/16 25%
0/122 0%
Melanoma
5/210 2%
43/1899 2%
Endometrial Carcinoma
1/42 2%
13/612 2%
Non-Small Cell Lung Carcinoma
11/304 4%
16/1390 1%
Burkitts Lymphoma
3/32 9%
0/196 0%
Neuroendocrine Tumour
6/154 4%
3/577 1%
Colorectal Carcinoma
5/143 4%
34/3239 1%
Chondrosarcoma
0/14 0%
1/75 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Squamous Cell Lung Carcinoma
0/57 0%
9/810 1%
Bladder Carcinoma
0/58 0%
10/956 1%
Other Solid Cancers
0/94 0%
13/1515 1%
Gastric Carcinoma
5/74 7%
10/1809 1%
Glioma
0/52 0%
12/2127 1%
Medulloblastoma
0/0 0%
2/450 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Mesothelioma
1/62 2%
0/165 0%
Kidney Carcinoma
2/85 2%
6/1862 0%
Other Sarcomas
0/69 0%
3/699 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
7/2550 0%
Breast Carcinoma
2/144 1%
10/3264 0%
Non-Cancerous
0/104 0%
3/830 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Ovarian Carcinoma
0/109 0%
3/998 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in TEC 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 297 mutations in TEC

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