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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 STX3

check button Gene summary
Gene informationGene symbol

STX3

Gene ID

6809

Gene namesyntaxin 3
SynonymsSTX3A
Cytomap

11q12.1

Type of geneprotein-coding
Descriptionsyntaxin-3syntaxin 3A
Modification date20200327
UniProtAcc

A0A0C4DGE4,

A0A0J9YW33,

A0A286YF28,

E9PN33,

E9PQJ8,

Q13277,

Context

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

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Gene structures and expression levels for STX3

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

ENSG00000166900
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
CBDOWNENST00000633708.1STX3-207:protein_coding:STX32.835277e+01-1.143259e+001.236567e-048.868407e-04

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 STX3

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_124041chr1159793479:59793514:59795602:59795712:59800855:5980096259795602:59795712
exon_skip_14093chr1159773211:59773294:59788873:59788947:59790519:5979058659788873:59788947
exon_skip_183775chr1159773217:59773294:59787037:59787136:59788873:5978894759787037:59787136
exon_skip_194287chr1159795415:59795482:59797283:59797396:59800855:5980096259797283:59797396
exon_skip_204450chr1159787067:59787136:59788873:59788947:59790519:5979058659788873:59788947
exon_skip_249098chr1159793380:59793514:59795372:59795482:59797283:5979736659795372:59795482
exon_skip_255170chr1159793479:59793514:59795372:59795482:59800855:5980096259795372:59795482
exon_skip_59426chr1159773211:59773294:59787037:59787136:59788873:5978894759787037:59787136
exon_skip_5971chr1159793479:59793514:59795372:59795482:59797283:5979736659795372:59795482

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_14093Mayo_CB5.019512e-016.679032e-01-1.659520e-011.046592e-08


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Open reading frame (ORF) annotation in the exon skipping event for STX3

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
ENST0000033797959797283597973963UTR-3CDS
ENST000003379795978703759787136Frame-shift
ENST000003379795978887359788947In-frame
ENST000003379795979537259795482In-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
ENST0000033797959797283597973963UTR-3CDS
ENST000003379795978703759787136Frame-shift
ENST000003379795978887359788947In-frame
ENST000003379795979537259795482In-frame

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
ENST0000033797959797283597973963UTR-3CDS
ENST000003379795978703759787136Frame-shift
ENST000003379795978887359788947In-frame
ENST000003379795979537259795482In-frame

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Infer the effects of exon skipping event on protein functional features for STX3

p-ENSG00000166900_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
ENST00000337979331628959788873597889477638367296
ENST000003379793316289597953725979548212241333225262

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
ENST00000337979331628959788873597889477638367296
ENST000003379793316289597953725979548212241333225262

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
ENST00000337979331628959788873597889477638367296
ENST000003379793316289597953725979548212241333225262

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
Q1327772961289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277729632111Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q1327772968383Natural variantID=VAR_028189;Note=E->D;Dbxref=dbSNP:rs12282741
Q1327772968181Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q1327772961263Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q13277225262226262Alternative sequenceID=VSP_006340;Note=In isoform B. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10080545;Dbxref=PMID:10080545
Q132772252621289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277225262191253DomainNote=t-SNARE coiled-coil homology;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00202
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q132772252621263Topological 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
Q1327772961289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277729632111Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q1327772968383Natural variantID=VAR_028189;Note=E->D;Dbxref=dbSNP:rs12282741
Q1327772968181Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q1327772961263Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q13277225262226262Alternative sequenceID=VSP_006340;Note=In isoform B. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10080545;Dbxref=PMID:10080545
Q132772252621289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277225262191253DomainNote=t-SNARE coiled-coil homology;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00202
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q132772252621263Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255

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
Q1327772961289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277729632111Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q1327772968383Natural variantID=VAR_028189;Note=E->D;Dbxref=dbSNP:rs12282741
Q1327772968181Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q1327772961263Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q13277225262226262Alternative sequenceID=VSP_006340;Note=In isoform B. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10080545;Dbxref=PMID:10080545
Q132772252621289ChainID=PRO_0000210199;Note=Syntaxin-3
Q13277225262191253DomainNote=t-SNARE coiled-coil homology;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00202
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q13277225262250250Sequence conflictNote=T->S;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q132772252621263Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255


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3'-UTR located exon skipping events that lost miRNA binding sites in STX3

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 STX3

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 STX3

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 STX3

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 STX3

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value
CBTRA2Aexon_skip_14093-5.473822e-011.254084e-12
CBNUP42exon_skip_140935.134975e-014.657803e-11
CBTRA2Aexon_skip_204450-4.244806e-019.313444e-08
CBSRSF1exon_skip_204450-4.681549e-012.545056e-09
IFGPABPC3exon_skip_59426-5.146193e-011.698741e-02
PCCG3BP2exon_skip_140934.392522e-015.532460e-10
PCCPTBP1exon_skip_1942875.549332e-014.639102e-14
TCELAVL4exon_skip_59426-6.321825e-011.492645e-17
TCESRP1exon_skip_59426-4.521964e-011.131646e-08
TCNOVA1exon_skip_59426-5.554562e-014.131548e-13
TCMSI1exon_skip_1942875.190469e-012.133001e-10
TCELAVL4exon_skip_194287-7.410704e-014.530383e-24
TCMBNL1exon_skip_194287-4.308842e-012.785294e-07
TCKHDRBS2exon_skip_194287-7.600265e-016.593285e-26
TCKHDRBS3exon_skip_194287-6.932495e-014.482841e-20
TCRBM24exon_skip_194287-7.112635e-011.745368e-21
TCHNRNPA0exon_skip_194287-6.727729e-011.359805e-18
TCHNRNPDLexon_skip_194287-5.298866e-017.604861e-11
TCHNRNPDexon_skip_194287-6.286610e-019.030921e-16
TCNUP42exon_skip_194287-6.527674e-012.960497e-17
TCPTBP1exon_skip_1942874.701140e-011.467278e-08
TCSRSF9exon_skip_194287-4.190247e-016.319741e-07

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RelatedDrugs for STX3

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 STX3

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