IL3RA

Interleukin 3 receptor subunit alpha P26951 IL3RA_HUMAN
Protein Coding Chr X X;Y Swiss-Prot reviewed Entrez 3563
Mutations
381
CL 27 · Tissue 351
Samples
208
CL 24 · Tissue 182
Peptides
162
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
Mutations38127351
Samples20824182
Peptides16221142

Function

IL3RA · Interleukin 3 receptor subunit alpha

The protein encoded by this gene is an interleukin 3 specific subunit of a heterodimeric cytokine receptor. The receptor is comprised of a ligand specific alpha subunit and a signal transducing beta subunit shared by the receptors for interleukin 3 (IL3), colony stimulating factor 2 (CSF2/GM-CSF), and interleukin 5 (IL5). The binding of this protein to IL3 depends on the beta subunit. The beta subunit is activated by the ligand binding, and is required for the biological activities of IL3. This gene and the gene encoding the colony stimulating factor 2 receptor alpha chain (CSF2RA) form a cytokine receptor gene cluster in a X-Y pseudoautosomal region on chromosomes X or Y. Alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jun 2012].

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
ENST00000331035 P26951 224 152
ENST00000381469 P26951-2 157 107

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
X;Y
Entrez ID
Aliases
CD123IL-3R-alphaIL3RIL3RAYIL3RXIL3RY

Recurrent Mutations

All 152 amino-acid changes on canonical ENST00000331035 · 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 IL3RA · 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 IL3RA – 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%
19/612 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Cervical Carcinoma
0/35 0%
7/422 2%
Non-Small Cell Lung Carcinoma
6/304 2%
16/1390 1%
Melanoma
0/210 0%
23/1899 1%
Colorectal Carcinoma
1/143 1%
34/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
1/74 1%
13/1809 1%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Mesothelioma
1/62 2%
0/165 0%
Meningioma
0/3 0%
1/252 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Ovarian Carcinoma
0/109 0%
4/998 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
8/2550 0%
Prostate Carcinoma
1/13 8%
5/2105 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Breast Carcinoma
1/144 1%
7/3264 0%
Medulloblastoma
0/0 0%
1/450 0%
Non-Cancerous
1/104 1%
1/830 0%
Other Blood Cancers
0/61 0%
4/2725 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%

Mutation Distribution

Where IL3RA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL3RA 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 381 mutations in IL3RA

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