CCR6

C-C motif chemokine receptor 6 P51684 CCR6_HUMAN
Protein Coding Chr 6 6q27 Swiss-Prot reviewed Entrez 1235
Mutations
932
CL 104 · Tissue 808
Samples
238
CL 40 · Tissue 194
Peptides
162
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
Mutations932104808
Samples23840194
Peptides16225139

Function

CCR6 · C-C motif chemokine receptor 6

This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. The gene is preferentially expressed by immature dendritic cells and memory T cells. The ligand of this receptor is macrophage inflammatory protein 3 alpha (MIP-3 alpha). This receptor has been shown to be important for B-lineage maturation and antigen-driven B-cell differentiation, and it may regulate the migration and recruitment of dentritic and T cells during inflammatory and immunological responses. Alternatively spliced transcript variants that encode the same protein have been described for this gene. [provided by RefSeq, Jul 2008].

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
ENST00000341935 P51684 248 162
ENST00000349984 P51684 228 154
ENST00000400926 P51684 228 154
ENST00000643861 P51684 228 154

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q27
Entrez ID
Aliases
BN-1C-C CKR-6CC-CKR-6CCR-6CD196CKR-L3

Recurrent Mutations

All 162 amino-acid changes on canonical ENST00000341935 · 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 CCR6 · 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 CCR6 – 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%
Squamous Cell Lung Carcinoma
4/57 7%
12/810 1%
Endometrial Carcinoma
3/42 7%
9/612 1%
Germ Cell Tumour
2/25 8%
1/169 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
1/210 0%
22/1899 1%
Other Solid Cancers
0/94 0%
15/1515 1%
Non-Small Cell Lung Carcinoma
1/304 0%
14/1390 1%
Colorectal Carcinoma
4/143 3%
23/3239 1%
Esophageal Squamous Cell Carcinoma
4/51 8%
16/2550 1%
Non-Cancerous
4/104 4%
3/830 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Gastric Carcinoma
0/74 0%
13/1809 1%
Neuroendocrine Tumour
4/154 3%
1/577 0%
Kidney Carcinoma
0/85 0%
11/1862 1%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Mesothelioma
1/62 2%
0/165 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Other Sarcomas
1/69 1%
1/699 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
2/2534 0%
Glioma
0/52 0%
5/2127 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%

Mutation Distribution

Where CCR6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CCR6 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 932 mutations in CCR6

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