CD3E

CD3 epsilon subunit of T-cell receptor complex P07766 CD3E_HUMAN
Protein Coding Chr 11 11q23.3 Swiss-Prot reviewed Entrez 916
Mutations
201
CL 36 · Tissue 163
Samples
108
CL 25 · Tissue 81
Peptides
98
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
Mutations20136163
Samples1082581
Peptides981882

Function

CD3E · CD3 epsilon subunit of T-cell receptor complex

The protein encoded by this gene is the CD3-epsilon polypeptide, which together with CD3-gamma, -delta and -zeta, and the T-cell receptor alpha/beta and gamma/delta heterodimers, forms the T-cell receptor-CD3 complex. This complex plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. The genes encoding the epsilon, gamma and delta polypeptides are located in the same cluster on chromosome 11. The epsilon polypeptide plays an essential role in T-cell development. Defects in this gene cause immunodeficiency. This gene has also been linked to a susceptibility to type I diabetes in women. [provided by RefSeq, Jul 2008].

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
ENST00000361763 P07766 111 85
ENST00000528600 E9PSH8* 90 76

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q23.3
Entrez ID
Aliases
CD3epsilonIMD18T3ETCRE

Recurrent Mutations

All 85 amino-acid changes on canonical ENST00000361763 · 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 CD3E · 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 CD3E – 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
2/40 5%
0/0 0%
Endometrial Carcinoma
4/42 10%
4/612 1%
Glioblastoma
1/98 1%
0/0 0%
Mesothelioma
1/62 2%
1/165 1%
Melanoma
1/210 0%
15/1899 1%
Non-Small Cell Lung Carcinoma
3/304 1%
5/1390 0%
Gastric Carcinoma
0/74 0%
7/1809 0%
Ovarian Carcinoma
0/109 0%
4/998 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Other Solid Cancers
4/94 4%
1/1515 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Colorectal Carcinoma
1/143 1%
9/3239 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Breast Carcinoma
2/144 1%
6/3264 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
4/2534 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Glioma
0/52 0%
2/2127 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Neuroblastoma
1/87 1%
0/1331 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where CD3E is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CD3E 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 53 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 201 mutations in CD3E

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