MMP10

Matrix metallopeptidase 10 P09238 MMP10_HUMAN
Protein Coding Chr 11 11q22.2 Swiss-Prot reviewed Entrez 4319
Mutations
278
CL 58 · Tissue 218
Samples
270
CL 58 · Tissue 210
Peptides
208
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
Mutations27858218
Samples27058210
Peptides20834177

Function

MMP10 · Matrix metallopeptidase 10

This gene encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this 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. The encoded preproprotein is proteolytically processed to generate the mature protease. This secreted protease breaks down fibronectin, laminin, elastin, proteoglycan core protein, gelatins, and several types of collagen. The gene is part of a cluster of MMP genes on chromosome 11. [provided by RefSeq, Jan 2016].

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
ENST00000279441 P09238 278 208

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q22.2
Entrez ID
Aliases
SL-2STMY2

Recurrent Mutations

All 208 amino-acid changes on canonical ENST00000279441 · 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 MMP10 · 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 MMP10 – 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
3/42 7%
13/612 2%
Chondrosarcoma
2/14 14%
0/75 0%
Melanoma
7/210 3%
36/1899 2%
Non-Small Cell Lung Carcinoma
14/304 5%
20/1390 1%
Neuroendocrine Tumour
7/154 5%
3/577 1%
Cervical Carcinoma
2/35 6%
4/422 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Colorectal Carcinoma
8/143 6%
19/3239 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Gastric Carcinoma
0/74 0%
14/1809 1%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Head and Neck Carcinoma
1/85 1%
8/1574 1%
Other Sarcomas
0/69 0%
4/699 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Glioma
0/52 0%
11/2127 1%
Thyroid Gland Carcinoma
2/45 4%
6/1592 0%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Ovarian Carcinoma
2/109 2%
3/998 0%
Hepatocellular Carcinoma
1/46 2%
8/2210 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Kidney Carcinoma
2/85 2%
4/1862 0%
Medulloblastoma
0/0 0%
1/450 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Pancreatic Carcinoma
1/89 1%
2/1611 0%
Breast Carcinoma
0/144 0%
5/3264 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%

Mutation Distribution

Where MMP10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in MMP10 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 22 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 278 mutations in MMP10

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