DUSP1

Dual specificity phosphatase 1 P28562 DUS1_HUMAN
Protein Coding Chr 5 5q35.1 Swiss-Prot reviewed Entrez 1843
Mutations
145
CL 26 · Tissue 117
Samples
141
CL 25 · Tissue 114
Peptides
108
unique mutant peptides
Transcripts
1
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
Mutations14526117
Samples14125114
Peptides1081990

Function

DUSP1 · Dual specificity phosphatase 1

The protein encoded by this gene is a phosphatase with dual specificity for tyrosine and threonine. The encoded protein can dephosphorylate MAP kinase MAPK1/ERK2, which results in its involvement in several cellular processes. This protein appears to play an important role in the human cellular response to environmental stress as well as in the negative regulation of cellular proliferation. Finally, the encoded protein can make some solid tumors resistant to both chemotherapy and radiotherapy, making it a target for cancer therapy. [provided by RefSeq, Aug 2017].

Isoforms & Proteins

1 transcript · 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
ENST00000239223 P28562 145 108

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5q35.1
Entrez ID
Aliases
CL100HVH1MKP-1MKP1PTPN10

Recurrent Mutations

All 108 amino-acid changes on canonical ENST00000239223 · 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 DUSP1 · 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 DUSP1 – 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
3/25 12%
0/0 0%
Endometrial Carcinoma
4/42 10%
4/612 1%
Other Solid Cancers
2/94 2%
14/1515 1%
Other Sarcomas
4/69 6%
2/699 0%
Bladder Carcinoma
0/58 0%
7/956 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Melanoma
1/210 0%
10/1899 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Osteosarcoma
1/45 2%
0/166 0%
Ovarian Carcinoma
1/109 1%
4/998 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Colorectal Carcinoma
0/143 0%
13/3239 0%
Non-Small Cell Lung Carcinoma
4/304 1%
2/1390 0%
Gastric Carcinoma
3/74 4%
3/1809 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
8/2550 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%
Glioma
0/52 0%
5/2127 0%
Non-Cancerous
0/104 0%
2/830 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
5/2534 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%

Mutation Distribution

Where DUSP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DUSP1 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 145 mutations in DUSP1

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