MAFK

MAF bZIP transcription factor K O60675 MAFK_HUMAN
Protein Coding Chr 7 7p22.3 Swiss-Prot reviewed Entrez 7975
Mutations
66
CL 16 · Tissue 49
Samples
64
CL 15 · Tissue 48
Peptides
44
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
Mutations661649
Samples641548
Peptides441333

Function

MAFK · MAF bZIP transcription factor K

The developmentally regulated expression of the globin genes depends on upstream regulatory elements termed locus control regions (LCRs). LCRs are associated with powerful enhancer activity that is mediated by the transcription factor NFE2 (nuclear factor erythroid-2). NFE2 recognition sites are also present in the gene promoters of 2 heme biosynthetic enzymes, porphobilinogen deaminase (PBGD; MIM 609806) and ferrochelatase (FECH; MIM 612386). NFE2 DNA-binding activity consists of a heterodimer containing an 18-kD Maf protein (MafF, MafG (MIM 602020), or MafK) and p45 (MIM 601490). Both subunits are members of the activator protein-1 superfamily of basic leucine zipper (bZIP) proteins (see MIM 165160). Maf homodimers suppress transcription at NFE2 sites.[supplied by OMIM, Nov 2008].

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
ENST00000343242 O60675 66 44

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p22.3
Entrez ID
Aliases
NFE2UP18

Recurrent Mutations

All 44 amino-acid changes on canonical ENST00000343242 · 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 MAFK · 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 MAFK – 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%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
6/612 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Colorectal Carcinoma
7/143 5%
11/3239 0%
Melanoma
2/210 1%
6/1899 0%
Non-Cancerous
0/104 0%
3/830 0%
Glioma
0/52 0%
5/2127 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Neuroblastoma
0/87 0%
2/1331 0%
Other Sarcomas
0/69 0%
1/699 0%
Pancreatic Carcinoma
1/89 1%
1/1611 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Non-Small Cell Lung Carcinoma
0/304 0%
2/1390 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Other Blood Cancers
1/61 2%
0/2725 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MAFK 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 66 mutations in MAFK

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