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Center for Computational Systems Medicine
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Gene summary

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Gene structures and expression levels

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Exon skipping events with PSIs in RPSMAP, MSBB, and Mayo

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Open reading frame (ORF) annotation in the exon skipping event

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Exon skipping events in the canonical protein sequence

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3'-UTR located exon skipping events lost miRNA binding sites

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SNVs in the skipped exons with depth of coverage

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AD stage-associated exon skipping events

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Correlation with RNA binding proteins (RBPs)

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Related drugs with this gene

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Related diseases with this gene

Gene summary for MET

check button Gene summary
Gene informationGene symbol

MET

Gene ID

4233

Gene nameMET proto-oncogene, receptor tyrosine kinase
SynonymsAUTS9|DFNB97|HGFR|RCCP2|c-Met
Cytomap

7q31.2

Type of geneprotein-coding
Descriptionhepatocyte growth factor receptorHGF receptorHGF/SF receptorSF receptorproto-oncogene c-Metscatter factor receptortyrosine-protein kinase Met
Modification date20200315
UniProtAcc

A0A024R728,

A0A024R759,

A0PJF7,

B5A929,

B5A930,

B5A931,

B5A933,

B5A934,

B5A935,

B5A936,

B5A937,

B5A938,

B5A939,

B5A940,

B5A941,

B5A942,

B5A943,

C9JKM5,

H7C130,

H7C174,

P08581,

Q14825,

Q9UEJ3,

Context

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
MET

GO:0001886

endothelial cell morphogenesis

14500721

MET

GO:0035024

negative regulation of Rho protein signal transduction

25198505

MET

GO:0045944

positive regulation of transcription by RNA polymerase II

22521434

MET

GO:0050918

positive chemotaxis

15218527

MET

GO:0051497

negative regulation of stress fiber assembly

25198505

MET

GO:0070495

negative regulation of thrombin-activated receptor signaling pathway

25198505

MET

GO:0071526

semaphorin-plexin signaling pathway

15218527

MET

GO:1905098

negative regulation of guanyl-nucleotide exchange factor activity

25198505


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Gene structures and expression levels for MET

check buttonSkipped exons in the ROSMAP, MSBB, and Mayo based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

ENSG00000105976
check button Differentially expressed gene analysis across multiple brain tissues between AD and control.
Tissue typeDEG directionBase mean exp.log2FC(AD/control)P-valueAdj. p-value

check button Differentially expressed isoform analysis across multiple brain tissues between AD and control.
gencode gene structure
Tissue typeDEG directionENSTTranscript info.Base mean exp.log2FC(AD/control)P-valueAdjc. p-value
CBUPENST00000318493.11MET-201:protein_coding:MET1.792197e+004.134321e+004.678261e-031.863589e-02

check button Landscape of isoform expressions across multiple brain tissues between AD and control.
gencode gene structure

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Exon skipping events with PSIs in ROSMAP, MSBB, and Mayo for MET

check button Landscape of individual exon skipping event across AD tissues and controls (PSI heatmap).
boxplot

check button All exon skipping events in AD cohorts.
Exon skip IDchrExons involved in exon skippingSkipped exon
exon_skip_128004chr7116672392:116672577:116699071:116700284:116731668:116731859116699071:116700284
exon_skip_191695chr7116672392:116672577:116695750:116695799:116699071:116699599116695750:116695799
exon_skip_216784chr7116758517:116758620:116759337:116759490:116763050:116763080116759337:116759490
exon_skip_248797chr7116672390:116672577:116695750:116695799:116699071:116699599116695750:116695799
exon_skip_257363chr7116758517:116758620:116759391:116759490:116763050:116763080116759391:116759490
exon_skip_258249chr7116771498:116771654:116771849:116771989:116774881:116775072116771849:116771989

check button Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control.
Exon skipping informationTissue typeAvg(PSIs) in ADAvg(PSIs) in controlDifference (PSI)Adj. p-value


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Open reading frame (ORF) annotation in the exon skipping event for MET

check button Open reading frame (ORF) of individual exon skipping events in ROSMAP based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000003977521166990711167002845CDS-5UTR
ENST00000397752116759391116759490Frame-shift
ENST00000397752116771849116771989In-frame

check button Open reading frame (ORF) of individual exon skipping events in MSBB based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000003977521166990711167002845CDS-5UTR
ENST00000397752116759391116759490Frame-shift

check button Open reading frame (ORF) of individual exon skipping events in Mayo based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000003977521166990711167002845CDS-5UTR
ENST00000397752116759391116759490Frame-shift

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Infer the effects of exon skipping event on protein functional features for MET

p-ENSG00000105976_img4.png
boxplot

check button Loci of skipped exons in ROSMAP across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST0000039775266521390116771849116771989308932289631009

check button Loci of skipped exons in MSBB across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end

check button Loci of skipped exons in Mayo across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end

check button Lost protein functional features of individual exon skipping events in ROSMAP.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
P0858196310097651390Alternative sequenceID=VSP_042448;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:18593464;Dbxref=PMID:18593464
P085819631009251390ChainID=PRO_0000024440;Note=Hepatocyte growth factor receptor
P085819631009966966Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:24275569;Dbxref=PMID:24275569
P085819631009977977Modified residueNote=Phosphothreonine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:18691976;Dbxref=PMID:18691976
P085819631009990990Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:23186163;Dbxref=PMID:18669648,PMID:23186163
P085819631009997997Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:18669648;Dbxref=PMID:18669648
P08581963100910001000Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:18669648;Dbxref=PMID:18669648
P08581963100910031003Modified residueNote=Phosphotyrosine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18691976,ECO:0000244|PubMed:19369195;Dbxref=PMID:18691976,PMID:19369195
P0858196310099641010Natural variantID=VAR_076584;Note=In OSFD%3B loss of CBL-mediated destabilization. Missing;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26637977;Dbxref=PMID:26637977
P085819631009970970Natural variantID=VAR_032482;Note=R->C;Ontology_term=ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:17053076,ECO:0000269|PubMed:17344846;Dbxref=dbSNP:rs34589476,PMID:17053076,PMID:17344846
P085819631009991991Natural variantID=VAR_032483;Note=In gastric cancer%3B prolonged tyrosine phosphorylation in response to HGF/SF%3B transforming activity in athymic nude mice. P->S;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:11042681;Dbxref=dbSNP:rs768678989,PMID:11042681
P085819631009992992Natural variantID=VAR_032484;Note=Found in a case of cancer of unknown primary origin%3B the mutated receptor is still functional and can sustain the transformed phenotype%3B somatic mutation. T->I;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=E
P08581963100910031003Natural variantID=VAR_076585;Note=Probable disease-associated mutation found in lesional sample from a patient with sporadically occurring%2C unilateral osteofibrous dysplasia%3B somatic mutation%3B complete loss of ligand-induced CBL-mediated ubiquitination%2C resultin
P08581963100910031003SiteNote=Required for ligand-induced CBL-mediated ubiquitination;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:12244174;Dbxref=PMID:12244174
P08581963100910091010SiteNote=Breakpoint for translocation to form TPR-MET oncogene
P0858196310099561390Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255

check button Lost protein functional features of individual exon skipping events in MSBB.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature

check button Lost protein functional features of individual exon skipping events in Mayo.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature


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3'-UTR located exon skipping events that lost miRNA binding sites in MET

check button 3'-UTR exon skipping evnets lost miRNA binding.
Tissue typeENSTExon skip startExon skip endmicroRNABinding site by TargetScanBinding type by TargetScanBdinding site by miRandaScore of miRandaEnergy by miRanda

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SNVs in the skipped exons for MET

check button - Differential PSIs between mutated versus non-mutated samples.

check button - Depth of Coverage in the skipped exon of the mutated samples.

check button - Sashimi plot in the skipped exon of the mutated samples.

check button - Non-synonymous mutations located in the skipped exons.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

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AD stage-associated exon skippint events for MET

check button Associated exon skipping events with Braak staging or Clinical Dementia Rating (CDR).
AD stage infoCohortTissueSE idCoefficient P-valueChromosomeStrandE1 startE1 endSkipped startSkipped endE2 startE2 end

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for MET

check button sQTL information located at the skipped exons.
Tissue typeExon skip IDSNP idLocationP-valueFDR

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Correlation with RNA binding proteins (RBPs) for MET

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value

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RelatedDrugs for MET

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
UniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
P08581approvedDB08865Crizotinibsmall moleculeP08581
P08581approved|investigationalDB08875Cabozantinibsmall moleculeP08581
P08581approved|investigationalDB12010Fostamatinibsmall moleculeP08581
P08581approved|investigationalDB12267Brigatinibsmall moleculeP08581

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RelatedDiseases for MET

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource