IL11RA

Interleukin 11 receptor subunit alpha Q14626 I11RA_HUMAN
Protein Coding Chr 9 9p13.3 Swiss-Prot reviewed Entrez 3590
Mutations
556
CL 92 · Tissue 462
Samples
163
CL 35 · Tissue 126
Peptides
135
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
Mutations55692462
Samples16335126
Peptides13525115

Function

IL11RA · Interleukin 11 receptor subunit alpha

Interleukin 11 is a stromal cell-derived cytokine that belongs to a family of pleiotropic and redundant cytokines that use the gp130 transducing subunit in their high affinity receptors. This gene encodes the IL-11 receptor, which is a member of the hematopoietic cytokine receptor family. This particular receptor is very similar to ciliary neurotrophic factor, since both contain an extracellular region with a 2-domain structure composed of an immunoglobulin-like domain and a cytokine receptor-like domain. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012].

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
ENST00000441545 Q14626 172 127
ENST00000318041 Q14626 150 116
ENST00000602473 Q14626-2 133 103
ENST00000555003 A0A8J9AZZ3* 101 76

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9p13.3
Entrez ID
Aliases
CRSDA

Recurrent Mutations

All 127 amino-acid changes on canonical ENST00000441545 · 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 IL11RA · 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 IL11RA – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Endometrial Carcinoma
2/42 5%
12/612 2%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Ovarian Carcinoma
3/109 3%
8/998 1%
Colorectal Carcinoma
5/143 4%
24/3239 1%
Melanoma
0/210 0%
18/1899 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Non-Small Cell Lung Carcinoma
4/304 1%
6/1390 0%
Gastric Carcinoma
5/74 7%
6/1809 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Neuroendocrine Tumour
0/154 0%
3/577 1%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
Non-Cancerous
0/104 0%
3/830 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Hepatocellular Carcinoma
1/46 2%
6/2210 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Bladder Carcinoma
0/58 0%
2/956 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
3/2534 0%
Glioma
0/52 0%
4/2127 0%
Breast Carcinoma
0/144 0%
6/3264 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
3/2550 0%
Neuroblastoma
1/87 1%
1/1331 0%
Other Sarcomas
0/69 0%
1/699 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Solid Cancers
1/94 1%
1/1515 0%
Prostate Carcinoma
0/13 0%
2/2105 0%

Mutation Distribution

Where IL11RA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL11RA 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 556 mutations in IL11RA

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