IL24

Interleukin 24 Q13007 IL24_HUMAN
Protein Coding Chr 1 1q32.1 Swiss-Prot reviewed Entrez 11009
Mutations
292
CL 48 · Tissue 244
Samples
112
CL 24 · Tissue 88
Peptides
108
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
Mutations29248244
Samples1122488
Peptides1081794

Function

IL24 · Interleukin 24

This gene encodes a member of the IL10 family of cytokines. It was identified as a gene induced during terminal differentiation in melanoma cells. The protein encoded by this gene can induce apoptosis selectively in various cancer cells. Overexpression of this gene leads to elevated expression of several GADD family genes, which correlates with the induction of apoptosis. The phosphorylation of mitogen-activated protein kinase 14 (MAPK7/P38), and heat shock 27kDa protein 1 (HSPB2/HSP27) are found to be induced by this gene in melanoma cells, but not in normal immortal melanocytes. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008].

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
ENST00000294984 Q13007 108 79
ENST00000391929 Q13007-2 95 78
ENST00000367093 Q13007-3 63 52
ENST00000611909 Q13007-4 26 19

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q32.1
Entrez ID
Aliases
C49AFISPIL10BMDA7MOB5ST16

Recurrent Mutations

All 79 amino-acid changes on canonical ENST00000294984 · 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 IL24 · 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 IL24 – 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
1/40 2%
0/0 0%
Endometrial Carcinoma
0/42 0%
11/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Colorectal Carcinoma
13/143 9%
13/3239 0%
Cervical Carcinoma
2/35 6%
1/422 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Non-Small Cell Lung Carcinoma
1/304 0%
6/1390 0%
Melanoma
1/210 0%
7/1899 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Non-Cancerous
1/104 1%
2/830 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Ovarian Carcinoma
0/109 0%
3/998 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Breast Carcinoma
2/144 1%
7/3264 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Thyroid Gland Carcinoma
1/45 2%
2/1592 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Glioma
0/52 0%
2/2127 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Neuroblastoma
0/87 0%
1/1331 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
Other Blood Cancers
0/61 0%
1/2725 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where IL24 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in IL24 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 53 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 292 mutations in IL24

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