CD27

CD27 molecule P26842 CD27_HUMAN
Protein Coding Chr 12 12p13.31 Swiss-Prot reviewed Entrez 939
Mutations
129
CL 14 · Tissue 112
Samples
122
CL 14 · Tissue 105
Peptides
86
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
Mutations12914112
Samples12214105
Peptides86977

Function

CD27 · CD27 molecule

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is required for generation and long-term maintenance of T cell immunity. It binds to ligand CD70, and plays a key role in regulating B-cell activation and immunoglobulin synthesis. This receptor transduces signals that lead to the activation of NF-kappaB and MAPK8/JNK. Adaptor proteins TRAF2 and TRAF5 have been shown to mediate the signaling process of this receptor. CD27-binding protein (SIVA), a proapoptotic protein, can bind to this receptor and is thought to play an important role in the apoptosis induced by this receptor. [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
ENST00000266557 P26842 129 86

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p13.31
Entrez ID
Aliases
S152S152. LPFS2T14TNFRSF7Tp55

Recurrent Mutations

All 86 amino-acid changes on canonical ENST00000266557 · 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 CD27 · 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 CD27 – 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%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Rhabdomyosarcoma
0/33 0%
3/171 2%
Bladder Carcinoma
1/58 2%
11/956 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Endometrial Carcinoma
0/42 0%
5/612 1%
Colorectal Carcinoma
6/143 4%
15/3239 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
0/104 0%
4/830 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Other Solid Cancers
1/94 1%
5/1515 0%
Melanoma
0/210 0%
7/1899 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Ovarian Carcinoma
2/109 2%
1/998 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Other Sarcomas
0/69 0%
2/699 0%
Glioma
0/52 0%
5/2127 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Wilms Tumour
0/5 0%
1/474 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Non-Small Cell Lung Carcinoma
0/304 0%
3/1390 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Other Blood Cancers
0/61 0%
2/2725 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where CD27 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CD27 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 129 mutations in CD27

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