MAPKBP1

Mitogen-activated protein kinase binding protein 1 O60336 MABP1_HUMAN
Protein Coding Chr 15 15q15.1 Swiss-Prot reviewed Entrez 23005
Mutations
1,856
CL 249 · Tissue 1,552
Samples
634
CL 117 · Tissue 500
Peptides
495
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
Mutations1,8562491,552
Samples634117500
Peptides49585417

Function

MAPKBP1 · Mitogen-activated protein kinase binding protein 1

This gene encodes a scaffold protein that regulates the JNK (c-Jun N-terminal kinase) and NOD2 (nucleotide-binding oligomerization domain-containing protein 2) signaling pathways. The encoded protein interacts with another related JNK pathway scaffold protein, WDR62, via a conserved dimerization domain, and enhances JNK signaling. This protein may play a role in bacterial immunity by binding to the NOD2 receptor and negatively regulating downstream antibacterial and pro-inflammatory signaling. Mutations in this gene that impair cellular localization of the encoded protein cause a form of nephronophthisis, an autosomal-recessive kidney disorder, in human patients. [provided by RefSeq, May 2017].

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
ENST00000457542 O60336-6 696 468
ENST00000456763 O60336 634 449
ENST00000514566 O60336-2 500 362
ENST00000627631 D6RAI2* 26 21

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q15.1
Entrez ID
Aliases
JNKBP-1JNKBP1NPHP20

Recurrent Mutations

All 468 amino-acid changes on canonical ENST00000457542 · 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 MAPKBP1 · 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 MAPKBP1 – 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
8/40 20%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Melanoma
13/210 6%
83/1899 4%
Endometrial Carcinoma
7/42 17%
21/612 3%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Glioblastoma
3/98 3%
0/0 0%
Colorectal Carcinoma
16/143 11%
61/3239 2%
Gastric Carcinoma
3/74 4%
36/1809 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Non-Small Cell Lung Carcinoma
6/304 2%
24/1390 2%
Other Solid Cancers
2/94 2%
26/1515 2%
Ovarian Carcinoma
5/109 5%
12/998 1%
Squamous Cell Lung Carcinoma
3/57 5%
10/810 1%
Neuroendocrine Tumour
4/154 3%
7/577 1%
Bladder Carcinoma
0/58 0%
15/956 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Non-Cancerous
2/104 2%
11/830 1%
Mesothelioma
3/62 5%
0/165 0%
Cervical Carcinoma
1/35 3%
5/422 1%
Head and Neck Carcinoma
2/85 2%
19/1574 1%
Esophageal Squamous Cell Carcinoma
4/51 8%
29/2550 1%
Other Sarcomas
4/69 6%
5/699 1%
Hepatocellular Carcinoma
0/46 0%
25/2210 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Biliary Tract Carcinoma
1/54 2%
9/950 1%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Burkitts Lymphoma
1/32 3%
1/196 1%
Glioma
0/52 0%
19/2127 1%
Plasma Cell Myeloma
0/44 0%
3/305 1%
Prostate Carcinoma
2/13 15%
15/2105 1%

Mutation Distribution

Where MAPKBP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MAPKBP1 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 1,856 mutations in MAPKBP1

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