MAP3K8

Mitogen-activated protein kinase kinase kinase 8 P41279 M3K8_HUMAN
Protein Coding Chr 10 10p11.23 Swiss-Prot reviewed Entrez 1326
Mutations
658
CL 66 · Tissue 577
Samples
213
CL 31 · Tissue 176
Peptides
160
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
Mutations65866577
Samples21331176
Peptides16021140

Function

MAP3K8 · Mitogen-activated protein kinase kinase kinase 8

This gene is an oncogene that encodes a member of the serine/threonine protein kinase family. The encoded protein localizes to the cytoplasm and can activate both the MAP kinase and JNK kinase pathways. This protein was shown to activate IkappaB kinases, and thus induce the nuclear production of NF-kappaB. This protein was also found to promote the production of TNF-alpha and IL-2 during T lymphocyte activation. This gene may also utilize a downstream in-frame translation start codon, and thus produce an isoform containing a shorter N-terminus. The shorter isoform has been shown to display weaker transforming activity. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011].

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
ENST00000263056 P41279 215 150
ENST00000375321 P41279 198 143
ENST00000542547 P41279 198 143
ENST00000375322 Q5T854* 47 36

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p11.23
Entrez ID
Aliases
AURA2COTESTESTFMEKK8TPL2

Recurrent Mutations

All 150 amino-acid changes on canonical ENST00000263056 · 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 MAP3K8 · 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 MAP3K8 – 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
4/42 10%
18/612 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Colorectal Carcinoma
6/143 4%
34/3239 1%
Melanoma
2/210 1%
21/1899 1%
Non-Small Cell Lung Carcinoma
3/304 1%
11/1390 1%
Ovarian Carcinoma
3/109 3%
5/998 0%
Bladder Carcinoma
0/58 0%
7/956 1%
Kidney Carcinoma
2/85 2%
11/1862 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Glioma
0/52 0%
10/2127 0%
Gastric Carcinoma
1/74 1%
7/1809 0%
Breast Carcinoma
2/144 1%
11/3264 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
Thyroid Gland Carcinoma
0/45 0%
5/1592 0%
Other Sarcomas
1/69 1%
1/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Medulloblastoma
0/0 0%
1/450 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Non-Cancerous
0/104 0%
2/830 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
2/2550 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
2/2534 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where MAP3K8 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MAP3K8 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 658 mutations in MAP3K8

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