IL10RA

Interleukin 10 receptor subunit alpha Q13651 I10R1_HUMAN
Protein Coding Chr 11 11q23.3 Swiss-Prot reviewed Entrez 3587
Mutations
323
CL 78 · Tissue 239
Samples
306
CL 71 · Tissue 231
Peptides
226
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
Mutations32378239
Samples30671231
Peptides22647180

Function

IL10RA · Interleukin 10 receptor subunit alpha

The protein encoded by this gene is a receptor for interleukin 10. This protein is structurally related to interferon receptors. It has been shown to mediate the immunosuppressive signal of interleukin 10, and thus inhibits the synthesis of proinflammatory cytokines. This receptor is reported to promote survival of progenitor myeloid cells through the insulin receptor substrate-2/PI 3-kinase/AKT pathway. Activation of this receptor leads to tyrosine phosphorylation of JAK1 and TYK2 kinases. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Jan 2009].

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
ENST00000227752 Q13651 323 226

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q23.3
Entrez ID
Aliases
CD210CD210aCDW210AHIL-10RIL-10R1IL10R

Recurrent Mutations

All 226 amino-acid changes on canonical ENST00000227752 · 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 IL10RA · 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 IL10RA – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Glioblastoma
3/98 3%
0/0 0%
Unknown
0/10 0%
1/29 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Melanoma
8/210 4%
39/1899 2%
Endometrial Carcinoma
0/42 0%
13/612 2%
Rhabdomyosarcoma
2/33 6%
1/171 1%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Colorectal Carcinoma
16/143 11%
27/3239 1%
Non-Small Cell Lung Carcinoma
8/304 3%
13/1390 1%
Other Solid Cancers
1/94 1%
18/1515 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Gastric Carcinoma
5/74 7%
13/1809 1%
Squamous Cell Lung Carcinoma
4/57 7%
4/810 0%
Mesothelioma
2/62 3%
0/165 0%
Non-Cancerous
2/104 2%
6/830 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Other Sarcomas
3/69 4%
3/699 0%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Small Cell Lung Carcinoma
1/9 11%
4/752 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Kidney Carcinoma
1/85 1%
9/1862 0%
Ovarian Carcinoma
4/109 4%
1/998 0%
Hepatocellular Carcinoma
0/46 0%
10/2210 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
8/2534 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
8/2550 0%

Mutation Distribution

Where IL10RA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL10RA 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 323 mutations in IL10RA

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