IL20RA

Interleukin 20 receptor subunit alpha Q9UHF4 I20RA_HUMAN
Protein Coding Chr 6 6q23.3 Swiss-Prot reviewed Entrez 53832
Mutations
937
CL 124 · Tissue 801
Samples
320
CL 62 · Tissue 253
Peptides
234
unique mutant peptides
Transcripts
4
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
Mutations937124801
Samples32062253
Peptides23444194

Function

IL20RA · Interleukin 20 receptor subunit alpha

This gene encodes a member of the type II cytokine receptor family. The encoded protein is a subunit of the receptor for interleukin 20, a cytokine that may be involved in epidermal function. The interleukin 20 receptor is a heterodimeric complex consisting of the encoded protein and interleukin 20 receptor beta. This gene and interleukin 20 receptor beta are highly expressed in skin, and are upregulated in psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013].

Isoforms & Proteins

4 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
ENST00000316649 Q9UHF4 328 209
ENST00000541547 Q9UHF4-3 276 183
ENST00000367748 Q9UHF4-2 233 160
ENST00000367746 Q96SH7* 100 66

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q23.3
Entrez ID
Aliases
CRF2-8IL-20R-alphaIL-20R1IL-20RA

Recurrent Mutations

All 209 amino-acid changes on canonical ENST00000316649 · 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 IL20RA · 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 IL20RA – 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-Lymphoblastic Leukemia
5/40 12%
0/0 0%
Chronic Myelogenous Leukemia
3/25 12%
0/0 0%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Melanoma
3/210 1%
67/1899 4%
Endometrial Carcinoma
1/42 2%
10/612 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
6/143 4%
31/3239 1%
Gastric Carcinoma
0/74 0%
20/1809 1%
Bladder Carcinoma
2/58 3%
8/956 1%
Non-Small Cell Lung Carcinoma
11/304 4%
5/1390 0%
Other Solid Cancers
1/94 1%
13/1515 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Sarcomas
2/69 3%
3/699 0%
Hepatocellular Carcinoma
0/46 0%
14/2210 1%
Head and Neck Carcinoma
5/85 6%
5/1574 0%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Osteosarcoma
0/45 0%
1/166 1%
Glioma
0/52 0%
10/2127 0%
Pancreatic Carcinoma
3/89 3%
4/1611 0%
Meningioma
0/3 0%
1/252 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%

Mutation Distribution

Where IL20RA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL20RA 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 937 mutations in IL20RA

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