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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 MAGI1

check button Gene summary
Gene informationGene symbol

MAGI1

Gene ID

9223

Gene namemembrane associated guanylate kinase, WW and PDZ domain containing 1
SynonymsAIP-3|AIP3|BAIAP1|BAP-1|BAP1|MAGI-1|MAGI-1b|Magi1d|TNRC19|WWP3
Cytomap

3p14.1

Type of geneprotein-coding
Descriptionmembrane-associated guanylate kinase, WW and PDZ domain-containing protein 1BAI1-associated protein 1WW domain-containing protein 3atrophin-1-interacting protein 3membrane-associated guanylate kinase inverted 1trinucleotide repeat-containing gene 19
Modification date20200313
UniProtAcc

A0A087WT53,

A0A087WXD2,

H7C4S7,

H7C4U7,

H7C535,

H7C5T8,

Q6P9H4,

Context

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
MAGI1

GO:0022409

positive regulation of cell-cell adhesion

20298433


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Gene structures and expression levels for MAGI1

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

ENSG00000151276
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
CBUPENST00000621418.4MAGI1-218:protein_coding:MAGI11.501767e+021.619080e+001.627911e-111.449857e-09
CBUPENST00000483466.5MAGI1-213:protein_coding:MAGI11.435524e+028.160124e-013.173894e-041.964475e-03
TCDOWNENST00000468159.1MAGI1-206:retained_intron:MAGI14.684734e+00-8.885793e-012.801480e-043.652705e-03
TCUPENST00000479287.1MAGI1-211:protein_coding:MAGI11.212643e+001.129818e+004.248954e-045.060339e-03

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 MAGI1

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_12741chr365356378:65357132:65359064:65359152:65361199:6536133765359064:65359152
exon_skip_139977chr365442792:65442849:65448022:65448057:65453258:6545334065448022:65448057
exon_skip_16089chr365387143:65387226:65391142:65391358:65401439:6540147065391142:65391358
exon_skip_164746chr365391142:65391358:65401439:65401470:65429520:6543014065401439:65401470
exon_skip_192224chr365391142:65391358:65401439:65401470:65429520:6542966565401439:65401470
exon_skip_192479chr365364853:65364946:65375745:65375948:65379261:6537955465375745:65375948
exon_skip_22306chr365448022:65448057:65453258:65453340:65470283:6547048465453258:65453340
exon_skip_228835chr365364853:65364946:65375745:65375945:65379261:6537955465375745:65375945
exon_skip_260776chr365493512:65493631:65609744:65609966:65621972:6562208865609744:65609966
exon_skip_76049chr365383532:65383623:65387143:65387226:65391142:6539135865387143:65387226
exon_skip_78443chr365439879:65440012:65442792:65442849:65453258:6545334065442792:65442849

check button Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control.
psi tcga
Exon skipping informationTissue typeAvg(PSIs) in ADAvg(PSIs) in controlDifference (PSI)Adj. p-value
exon_skip_12741Mayo_CB5.301220e-017.304478e-01-2.003258e-014.262950e-09
exon_skip_12741Mayo_TC6.113750e-017.498413e-01-1.384663e-012.426568e-06
exon_skip_76049Mayo_TC4.396341e-015.455882e-01-1.059541e-013.466118e-04


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Open reading frame (ORF) annotation in the exon skipping event for MAGI1

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

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

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

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Infer the effects of exon skipping event on protein functional features for MAGI1

p-ENSG00000151276_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

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

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 MAGI1

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 MAGI1

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 MAGI1

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 MAGI1

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 MAGI1

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value
CBTARDBPexon_skip_12741-5.148883e-011.842619e-11
CBRBM6exon_skip_12741-5.486389e-014.371088e-13
CBFUBP1exon_skip_12741-5.294731e-013.848522e-12
CBHNRNPA2B1exon_skip_12741-5.104470e-012.925573e-11
CBRBM45exon_skip_127417.127993e-012.069455e-24
CBNUP42exon_skip_127415.981660e-017.930079e-16
CBHNRNPFexon_skip_12741-4.053936e-012.917074e-07
CBRBM4Bexon_skip_12741-4.653703e-012.232545e-09
CBNUP42exon_skip_760494.993532e-011.209709e-10
HCCRBFOX2exon_skip_127414.380611e-014.740010e-13
HCCHNRNPFexon_skip_12741-4.476824e-011.260023e-13
HCCZNF326exon_skip_76049-5.064022e-013.121055e-17
HCCRBM47exon_skip_76049-4.749190e-014.485006e-15
HCCHNRNPFexon_skip_76049-5.276373e-018.096127e-19
HCCRBM4Bexon_skip_76049-4.173759e-011.161744e-11
IFGTARDBPexon_skip_12741-4.563840e-012.183903e-02
IFGRBM47exon_skip_12741-4.573136e-012.153779e-02
IFGHNRNPFexon_skip_12741-4.274989e-013.304026e-02
PCCRBFOX2exon_skip_127414.876927e-012.523559e-12
PCCRBM6exon_skip_12741-4.051578e-011.276468e-08
PCCRBM47exon_skip_12741-5.272164e-011.755888e-14
PCCHNRNPFexon_skip_12741-4.276326e-011.562312e-09
PCCELAVL4exon_skip_2288354.045762e-014.882920e-08
PCCRBM47exon_skip_228835-4.142314e-012.160943e-08
PCCRBM47exon_skip_192479-4.274483e-012.169799e-09
PCCRBM47exon_skip_76049-4.988604e-012.757985e-13
PCCHNRNPFexon_skip_76049-4.211676e-011.591962e-09
TCRBFOX2exon_skip_127416.102739e-015.902530e-16
TCILF2exon_skip_127414.947685e-013.363403e-10
TCHNRNPDLexon_skip_127414.778865e-011.583561e-09
TCRBM45exon_skip_127414.969555e-012.734661e-10
TCNUP42exon_skip_127415.929408e-016.082063e-15
TCEWSR1exon_skip_127414.219900e-011.527075e-07
TCHNRNPH2exon_skip_127416.297588e-013.595414e-17
TCESRP1exon_skip_127414.890842e-015.720491e-10
TCNOVA1exon_skip_127417.222131e-012.460106e-24
TCNUP42exon_skip_760496.983722e-012.966992e-23

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RelatedDrugs for MAGI1

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
UniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for MAGI1

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