IL26

Interleukin 26 Q9NPH9 IL26_HUMAN
Protein Coding Chr 12 12q15 Swiss-Prot reviewed Entrez 55801
Mutations
86
CL 10 · Tissue 75
Samples
82
CL 10 · Tissue 71
Peptides
66
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
Mutations861075
Samples821071
Peptides66859

Function

IL26 · Interleukin 26

This gene was identified by its overexpression specifically in herpesvirus samimiri-transformed T cells. The encoded protein is a member of the IL10 family of cytokines. It is a secreted protein and may function as a homodimer. This protein is thought to contribute to the transformed phenotype of T cells after infection by herpesvirus samimiri. [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
ENST00000229134 Q9NPH9 86 66

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q15
Entrez ID
Aliases
AK155IL-26

Recurrent Mutations

All 66 amino-acid changes on canonical ENST00000229134 · 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 IL26 · 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 IL26 – 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
Endometrial Carcinoma
2/42 5%
5/612 1%
Non-Small Cell Lung Carcinoma
2/304 1%
11/1390 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Colorectal Carcinoma
2/143 1%
17/3239 1%
Melanoma
0/210 0%
9/1899 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Other Sarcomas
1/69 1%
1/699 0%
Other Solid Cancers
1/94 1%
3/1515 0%
Medulloblastoma
0/0 0%
1/450 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Glioma
0/52 0%
3/2127 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Breast Carcinoma
1/144 1%
1/3264 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%

Mutation Distribution

Where IL26 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL26 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 12 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 86 mutations in IL26

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