IL10

Interleukin 10 P22301 IL10_HUMAN
Protein Coding Chr 1 1q32.1 Swiss-Prot reviewed Entrez 3586
Mutations
85
CL 11 · Tissue 70
Samples
82
CL 11 · Tissue 67
Peptides
55
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
Mutations851170
Samples821167
Peptides55748

Function

IL10 · Interleukin 10

The protein encoded by this gene is a cytokine produced primarily by monocytes and to a lesser extent by lymphocytes. This cytokine has pleiotropic effects in immunoregulation and inflammation. It down-regulates the expression of Th1 cytokines, MHC class II Ags, and costimulatory molecules on macrophages. It also enhances B cell survival, proliferation, and antibody production. This cytokine can block NF-kappa B activity, and is involved in the regulation of the JAK-STAT signaling pathway. Knockout studies in mice suggested the function of this cytokine as an essential immunoregulator in the intestinal tract. Mutations in this gene are associated with an increased susceptibility to HIV-1 infection and rheumatoid arthritis. [provided by RefSeq, May 2020].

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
ENST00000423557 P22301 85 55

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q32.1
Entrez ID
Aliases
CSIFGVHDSIL-10IL10ATGIF

Recurrent Mutations

All 55 amino-acid changes on canonical ENST00000423557 · 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 IL10 · 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 IL10 – 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
Glioblastoma
2/98 2%
0/0 0%
Endometrial Carcinoma
3/42 7%
5/612 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Meningioma
0/3 0%
2/252 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Melanoma
1/210 0%
10/1899 1%
Colorectal Carcinoma
0/143 0%
13/3239 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Other Sarcomas
0/69 0%
2/699 0%
Non-Small Cell Lung Carcinoma
0/304 0%
4/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Thyroid Gland Carcinoma
1/45 2%
2/1592 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Glioma
0/52 0%
1/2127 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where IL10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL10 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 46 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 85 mutations in IL10

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