MET

MET proto-oncogene, receptor tyrosine kinase P08581 MET_HUMAN
Protein Coding Chr 7 7q31.2 Swiss-Prot reviewed Entrez 4233
Mutations
2,127
CL 240 · Tissue 1,865
Samples
794
CL 123 · Tissue 665
Peptides
634
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
Mutations2,1272401,865
Samples794123665
Peptides63488553

Function

MET · MET proto-oncogene, receptor tyrosine kinase

This gene encodes a member of the receptor tyrosine kinase family of proteins and the product of the proto-oncogene MET. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that are linked via disulfide bonds to form the mature receptor. Further processing of the beta subunit results in the formation of the M10 peptide, which has been shown to reduce lung fibrosis. Binding of its ligand, hepatocyte growth factor, induces dimerization and activation of the receptor, which plays a role in cellular survival, embryogenesis, and cellular migration and invasion. Mutations in this gene are associated with papillary renal cell carcinoma, hepatocellular carcinoma, and various head and neck cancers. Amplification and overexpression of this gene are also associated with multiple human cancers. [provided by RefSeq, May 2016].

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
ENST00000397752 P08581 873 612
ENST00000318493 P08581-2 809 586
ENST00000436117 P08581-3 443 331
ENST00000422097 A0ACM8QMG8* 2 2

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q31.2
Entrez ID
Aliases
AUTS9DA11DFNB97HGFRRCCP2c-Met

Recurrent Mutations

All 612 amino-acid changes on canonical ENST00000397752 · 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 MET · 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 MET – 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%
Gastrointestinal Stromal Tumour
0/0 0%
18/133 14%
Endometrial Carcinoma
8/42 19%
42/612 7%
Melanoma
9/210 4%
113/1899 6%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Non-Small Cell Lung Carcinoma
15/304 5%
33/1390 2%
Pheochromocytoma and Paraganglioma
0/0 0%
2/71 3%
Other Solid Cancers
3/94 3%
39/1515 3%
Bladder Carcinoma
0/58 0%
26/956 3%
Colorectal Carcinoma
19/143 13%
65/3239 2%
Other Sarcomas
2/69 3%
17/699 2%
Gastric Carcinoma
2/74 3%
33/1809 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Kidney Carcinoma
2/85 2%
34/1862 2%
Adrenocortical Carcinoma
0/3 0%
2/112 2%
Glioma
2/52 4%
35/2127 2%
Germ Cell Tumour
2/25 8%
1/169 1%
Rhabdomyosarcoma
2/33 6%
1/171 1%
Osteosarcoma
2/45 4%
1/166 1%
Squamous Cell Lung Carcinoma
5/57 9%
7/810 1%
Small Cell Lung Carcinoma
0/9 0%
10/752 1%
Hepatocellular Carcinoma
2/46 4%
26/2210 1%
Neuroendocrine Tumour
3/154 2%
6/577 1%
Biliary Tract Carcinoma
1/54 2%
11/950 1%
Ovarian Carcinoma
2/109 2%
11/998 1%
Chondrosarcoma
1/14 7%
0/75 0%
Prostate Carcinoma
1/13 8%
21/2105 1%
Esophageal Carcinoma
1/23 4%
7/769 1%
Esophageal Squamous Cell Carcinoma
4/51 8%
19/2550 1%
Cervical Carcinoma
2/35 6%
2/422 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in MET 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 2,127 mutations in MET

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