CD8A

CD8 subunit alpha P01732 CD8A_HUMAN
Protein Coding Chr 2 2p11.2 Swiss-Prot reviewed Entrez 925
Mutations
440
CL 36 · Tissue 396
Samples
123
CL 17 · Tissue 104
Peptides
111
unique mutant peptides
Transcripts
4
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
Mutations44036396
Samples12317104
Peptides1111697

Function

CD8A · CD8 subunit alpha

The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen acts as a coreceptor with the T-cell receptor on the T lymphocyte to recognize antigens displayed by an antigen presenting cell in the context of class I MHC molecules. The coreceptor functions as either a homodimer composed of two alpha chains or as a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 alpha chain. Multiple transcript variants encoding different isoforms have been found for this gene. The major protein isoforms of this gene differ by the presence or absence of a transmembrane domain and thus differ in being a membrane-anchored or secreted protein. [provided by RefSeq, May 2020].

Isoforms & Proteins

4 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
ENST00000283635 P01732 125 93
ENST00000409511 P01732 113 86
ENST00000352580 P01732-2 105 78
ENST00000409781 B8ZZZ4* 97 73

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p11.2
Entrez ID
Aliases
CD8CD8alphaIMD116Leu2p32

Recurrent Mutations

All 93 amino-acid changes on canonical ENST00000283635 · 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 CD8A · 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 CD8A – 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%
Glioblastoma
1/98 1%
0/0 0%
Endometrial Carcinoma
2/42 5%
3/612 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Gastric Carcinoma
0/74 0%
12/1809 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
14/2550 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Colorectal Carcinoma
2/143 1%
14/3239 0%
Melanoma
1/210 0%
9/1899 0%
Non-Small Cell Lung Carcinoma
3/304 1%
5/1390 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Ovarian Carcinoma
0/109 0%
4/998 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Glioma
0/52 0%
5/2127 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Thyroid Gland Carcinoma
1/45 2%
2/1592 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Non-Cancerous
0/104 0%
1/830 0%
Breast Carcinoma
0/144 0%
3/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where CD8A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CD8A 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 440 mutations in CD8A

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