DYRK4

Dual specificity tyrosine phosphorylation regulated kinase 4 Q9NR20 DYRK4_HUMAN
Protein Coding Chr 12 12p13.32 Swiss-Prot reviewed Entrez 8798
Mutations
1,002
CL 193 · Tissue 800
Samples
352
CL 89 · Tissue 259
Peptides
263
unique mutant peptides
Transcripts
3
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
Mutations1,002193800
Samples35289259
Peptides26359215

Function

DYRK4 · Dual specificity tyrosine phosphorylation regulated kinase 4

This gene encodes an enzyme that belongs to a conserved family of serine/threonine protein kinases. Members of this dual specificity kinase family are thought to function in the regulation of cell differentiation and proliferation, survival, and in development. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Aug 2013].

Isoforms & Proteins

3 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
ENST00000543431 A0A0A0MTH5* 362 244
ENST00000540757 Q9NR20 322 230
ENST00000010132 Q9NR20 318 227

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p13.32
Entrez ID

Recurrent Mutations

All 230 amino-acid changes on canonical ENST00000540757 · 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 DYRK4 · 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 DYRK4 – 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
8/42 19%
21/612 3%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Melanoma
2/210 1%
42/1899 2%
Non-Small Cell Lung Carcinoma
18/304 6%
17/1390 1%
Glioblastoma
2/98 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Other Sarcomas
5/69 7%
8/699 1%
Other Solid Cancers
2/94 2%
25/1515 2%
Colorectal Carcinoma
15/143 10%
37/3239 1%
Bladder Carcinoma
2/58 3%
10/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
9/810 1%
Cervical Carcinoma
3/35 9%
1/422 0%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Head and Neck Carcinoma
0/85 0%
13/1574 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Gastric Carcinoma
1/74 1%
13/1809 1%
Ovarian Carcinoma
5/109 5%
1/998 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Medulloblastoma
0/0 0%
2/450 0%
Breast Carcinoma
6/144 4%
9/3264 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Pancreatic Carcinoma
1/89 1%
6/1611 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Prostate Carcinoma
2/13 15%
6/2105 0%
Glioma
0/52 0%
8/2127 0%
Non-Cancerous
1/104 1%
2/830 0%
Hepatocellular Carcinoma
2/46 4%
4/2210 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
5/2550 0%

Mutation Distribution

Where DYRK4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DYRK4 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 1,002 mutations in DYRK4

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