IL6

Interleukin 6 P05231 IL6_HUMAN
Protein Coding Chr 7 7p15.3 Swiss-Prot reviewed Entrez 3569
Mutations
436
CL 52 · Tissue 376
Samples
106
CL 17 · Tissue 84
Peptides
101
unique mutant peptides
Transcripts
6
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
Mutations43652376
Samples1061784
Peptides1011583

Function

IL6 · Interleukin 6

This gene encodes a cytokine that functions in inflammation and the maturation of B cells. In addition, the encoded protein has been shown to be an endogenous pyrogen capable of inducing fever in people with autoimmune diseases or infections. The protein is primarily produced at sites of acute and chronic inflammation, where it is secreted into the serum and induces a transcriptional inflammatory response through interleukin 6 receptor, alpha. The functioning of this gene is implicated in a wide variety of inflammation-associated disease states, including suspectibility to diabetes mellitus and systemic juvenile rheumatoid arthritis. Elevated levels of the encoded protein have been found in virus infections, including COVID-19 (disease caused by SARS-CoV-2). [provided by RefSeq, Aug 2020].

Isoforms & Proteins

6 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
ENST00000258743 P05231 105 84
ENST00000404625 P05231 93 77
ENST00000401630 B5MCZ3* 84 70
ENST00000406575 B5MC14* 73 64
ENST00000407492 B5MC21* 50 42
ENST00000401651 B4DNV3* 31 30

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p15.3
Entrez ID
Aliases
BSF-2BSF2CDFHGFHSFIFN-beta-2

Recurrent Mutations

All 84 amino-acid changes on canonical ENST00000258743 · 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 IL6 · 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 IL6 – 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
Chordoma
1/7 14%
0/13 0%
Endometrial Carcinoma
0/42 0%
6/612 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Melanoma
1/210 0%
15/1899 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Colorectal Carcinoma
6/143 4%
15/3239 0%
Bladder Carcinoma
1/58 2%
5/956 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Osteosarcoma
1/45 2%
0/166 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Non-Small Cell Lung Carcinoma
2/304 1%
3/1390 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Glioma
0/52 0%
5/2127 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Other Blood Cancers
0/61 0%
4/2725 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Other Sarcomas
0/69 0%
1/699 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
B-Lymphoblastic Leukemia
1/55 2%
1/2640 0%
Neuroblastoma
0/87 0%
1/1331 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where IL6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL6 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 436 mutations in IL6

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