IL10RB

Interleukin 10 receptor subunit beta Q08334 I10R2_HUMAN
Protein Coding Chr 21 21q22.11 Swiss-Prot reviewed Entrez 3588
Mutations
192
CL 33 · Tissue 154
Samples
185
CL 32 · Tissue 148
Peptides
123
unique mutant peptides
Transcripts
2
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
Mutations19233154
Samples18532148
Peptides12324105

Function

IL10RB · Interleukin 10 receptor subunit beta

The protein encoded by this gene belongs to the cytokine receptor family. It is an accessory chain essential for the active interleukin 10 receptor complex. Coexpression of this and IL10RA proteins has been shown to be required for IL10-induced signal transduction. This gene and three other interferon receptor genes, IFAR2, IFNAR1, and IFNGR2, form a class II cytokine receptor gene cluster located in a small region on chromosome 21. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000290200 Q08334 191 122
ENST00000609556 A0A1B0GU52* 1 1

Gene Properties

Type
Protein Coding
Chromosome
21
Cytoband
21q22.11
Entrez ID
Aliases
CDW210BCRF2-4CRFB4D21S58D21S66IBD25

Recurrent Mutations

All 122 amino-acid changes on canonical ENST00000290200 · 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 IL10RB · 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 IL10RB – 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
T-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Rhabdomyosarcoma
0/33 0%
6/171 4%
Endometrial Carcinoma
3/42 7%
11/612 2%
Colorectal Carcinoma
4/143 3%
32/3239 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Melanoma
0/210 0%
18/1899 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Non-Small Cell Lung Carcinoma
3/304 1%
8/1390 1%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Gastric Carcinoma
0/74 0%
11/1809 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Meningioma
0/3 0%
1/252 0%
Breast Carcinoma
3/144 2%
9/3264 0%
Non-Cancerous
0/104 0%
3/830 0%
Hepatocellular Carcinoma
1/46 2%
6/2210 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Glioma
0/52 0%
4/2127 0%
Other Blood Cancers
2/61 3%
2/2725 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%
Kidney Carcinoma
1/85 1%
1/1862 0%
Prostate Carcinoma
0/13 0%
2/2105 0%

Mutation Distribution

Where IL10RB is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL10RB 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 192 mutations in IL10RB

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