TEAD4

TEA domain transcription factor 4 Q15561 TEAD4_HUMAN
Protein Coding Chr 12 12p13.33 Swiss-Prot reviewed Entrez 7004
Mutations
553
CL 49 · Tissue 500
Samples
213
CL 24 · Tissue 187
Peptides
175
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
Mutations55349500
Samples21324187
Peptides17519160

Function

TEAD4 · TEA domain transcription factor 4

This gene product is a member of the transcriptional enhancer factor (TEF) family of transcription factors, which contain the TEA/ATTS DNA-binding domain. It is preferentially expressed in the skeletal muscle, and binds to the M-CAT regulatory element found in promoters of muscle-specific genes to direct their gene expression. Alternatively spliced transcripts encoding distinct isoforms, some of which are translated through the use of a non-AUG (UUG) initiation codon, have been described for this gene. [provided by RefSeq, Jul 2008].

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
ENST00000359864 Q15561 221 161
ENST00000358409 Q15561-3 184 139
ENST00000397122 Q15561-2 148 113

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p13.33
Entrez ID
Aliases
EFTR-2RTEF1TCF13L1TEF-3TEF3TEFR-1

Recurrent Mutations

All 161 amino-acid changes on canonical ENST00000359864 · 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 TEAD4 · 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 TEAD4 – 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%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Endometrial Carcinoma
1/42 2%
13/612 2%
Melanoma
1/210 0%
29/1899 2%
Gastric Carcinoma
2/74 3%
20/1809 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Colorectal Carcinoma
4/143 3%
25/3239 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Cervical Carcinoma
1/35 3%
2/422 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
16/2550 1%
Non-Small Cell Lung Carcinoma
1/304 0%
8/1390 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Osteosarcoma
0/45 0%
1/166 1%
Ovarian Carcinoma
2/109 2%
3/998 0%
Hepatocellular Carcinoma
1/46 2%
9/2210 0%
Other Sarcomas
1/69 1%
2/699 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Neuroblastoma
1/87 1%
4/1331 0%
Glioma
0/52 0%
7/2127 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Breast Carcinoma
0/144 0%
8/3264 0%
Non-Cancerous
1/104 1%
1/830 0%
Wilms Tumour
0/5 0%
1/474 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Other Solid Cancers
0/94 0%
3/1515 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
2/2534 0%
Kidney Carcinoma
0/85 0%
3/1862 0%

Mutation Distribution

Where TEAD4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TEAD4 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 553 mutations in TEAD4

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