MMP23B

Matrix metallopeptidase 23B O75900 MMP23_HUMAN
Protein Coding Chr 1 1p36.33 Swiss-Prot reviewed Entrez 8510
Mutations
36
CL 12 · Tissue 23
Samples
27
CL 12 · Tissue 14
Peptides
27
unique mutant peptides
Transcripts
2
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
Mutations361223
Samples271214
Peptides271214

Function

MMP23B · Matrix metallopeptidase 23B

This gene (MMP23B) encodes a member of the matrix metalloproteinase (MMP) family, and it is part of a duplicated region of chromosome 1p36.3. Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. This gene belongs to the more telomeric copy of the duplicated region. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000356026 O75900 26 23
ENST00000378675 F6SAZ5* 10 7

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p36.33
Entrez ID
Aliases
MIFRMIFR-1MMP22

Recurrent Mutations

All 23 amino-acid changes on canonical ENST00000356026 · 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 MMP23B · 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 MMP23B – 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
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Glioblastoma
1/98 1%
0/0 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Medulloblastoma
0/0 0%
1/450 0%
Non-Cancerous
1/104 1%
1/830 0%
Other Solid Cancers
2/94 2%
1/1515 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Melanoma
0/210 0%
3/1899 0%
Gastric Carcinoma
1/74 1%
1/1809 0%
Bladder Carcinoma
1/58 2%
0/956 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Colorectal Carcinoma
1/143 1%
2/3239 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Hepatocellular Carcinoma
1/46 2%
0/2210 0%
Breast Carcinoma
1/144 1%
0/3264 0%

Mutation Distribution

Where MMP23B is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MMP23B 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 36 mutations in MMP23B

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