MAPK9

Mitogen-activated protein kinase 9 P45984 MK09_HUMAN
Protein Coding Chr 5 5q35.3 Swiss-Prot reviewed Entrez 5601
Mutations
1,122
CL 184 · Tissue 918
Samples
216
CL 42 · Tissue 168
Peptides
202
unique mutant peptides
Transcripts
8
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
Mutations1,122184918
Samples21642168
Peptides20231172

Function

MAPK9 · Mitogen-activated protein kinase 9

The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase targets specific transcription factors, and thus mediates immediate-early gene expression in response to various cell stimuli. It is most closely related to MAPK8, both of which are involved in UV radiation induced apoptosis, thought to be related to the cytochrome c-mediated cell death pathway. This gene and MAPK8 are also known as c-Jun N-terminal kinases. This kinase blocks the ubiquitination of tumor suppressor p53, and thus it increases the stability of p53 in nonstressed cells. Studies of this gene's mouse counterpart suggest a key role in T-cell differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Sep 2008].

Isoforms & Proteins

8 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
ENST00000452135 P45984 213 156
ENST00000455781 P45984-4 184 142
ENST00000393360 P45984-2 171 137
ENST00000343111 P45984-3 167 132
ENST00000347470 J3KNK1* 151 117
ENST00000425491 P45984-5 115 91
ENST00000539014 D7R525* 98 77
ENST00000397072 A0ACM8QKD3* 23 19

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5q35.3
Entrez ID
Aliases
JNK-55JNK2JNK2AJNK2ALPHAJNK2BJNK2BETA

Recurrent Mutations

All 156 amino-acid changes on canonical ENST00000452135 · 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 MAPK9 · 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 MAPK9 – 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%
12/612 2%
Cervical Carcinoma
0/35 0%
6/422 1%
Melanoma
3/210 1%
24/1899 1%
Colorectal Carcinoma
13/143 9%
25/3239 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Bladder Carcinoma
2/58 3%
6/956 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Thyroid Gland Carcinoma
0/45 0%
10/1592 1%
Glioma
0/52 0%
13/2127 1%
Gastric Carcinoma
0/74 0%
11/1809 1%
Non-Small Cell Lung Carcinoma
0/304 0%
9/1390 1%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Other Sarcomas
3/69 4%
1/699 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Head and Neck Carcinoma
2/85 2%
6/1574 0%
Ovarian Carcinoma
1/109 1%
4/998 0%
Mesothelioma
1/62 2%
0/165 0%
Other Solid Cancers
1/94 1%
5/1515 0%
Squamous Cell Lung Carcinoma
1/57 2%
2/810 0%
Non-Cancerous
0/104 0%
3/830 0%
Pancreatic Carcinoma
3/89 3%
2/1611 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Small Cell Lung Carcinoma
1/9 11%
1/752 0%
B-Lymphoblastic Leukemia
3/55 5%
1/2640 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Neuroblastoma
0/87 0%
2/1331 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Breast Carcinoma
0/144 0%
4/3264 0%

Mutation Distribution

Where MAPK9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MAPK9 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 1,122 mutations in MAPK9

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