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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 TCGA

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Exon skipping events with PSIs in GTEx

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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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SNVs in the skipped exons with depth of coverage

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

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Related drugs with this gene

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Related diseases with this gene

Gene summary for DEK

check button Gene summary
Gene informationGene symbol

DEK

Gene ID

7913

Gene nameDEK proto-oncogene
SynonymsD6S231E
Cytomap

6p22.3

Type of geneprotein-coding
Descriptionprotein DEKDEK oncogene (DNA binding)
Modification date20180527
UniProtAcc

P35659

ContextPubMed: DEK [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract]
- Title (PMID)

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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Exon skipping events across known transcript of Ensembl for DEK from UCSC genome browser

check buttonSkipped exons in TCGA and GTEx 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

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Gene isoform structures and expression levels for DEK

check button Expression levels of gene isoforms across TCGA.
gencode gene structure

check button Expression levels of gene isoforms across GTEx.
gencode gene structure


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Exon skipping events with PSIs in TCGA for DEK

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_456531618225841:18225961:18226404:18226473:18236682:1823682718226404:18226473ENSG00000124795.10ENST00000505224.1,ENST00000397239.3,ENST00000244776.7
exon_skip_456539618226404:18226473:18236682:18236831:18237611:1823774718236682:18236831ENSG00000124795.10ENST00000507591.1,ENST00000505224.1,ENST00000397239.3,ENST00000244776.7
exon_skip_456542618237611:18237747:18244738:18244834:18249881:1824991018244738:18244834ENSG00000124795.10ENST00000515770.1
exon_skip_456543618237611:18237747:18249881:18250070:18255961:1825608118249881:18250070ENSG00000124795.10ENST00000505224.1,ENST00000397239.3,ENST00000512145.1,ENST00000244776.7
exon_skip_456545618249881:18250070:18255961:18256082:18256591:1825660518255961:18256082ENSG00000124795.10ENST00000515770.1,ENST00000505224.1,ENST00000397239.3,ENST00000512145.1,ENST00000244776.7
exon_skip_456552618255966:18256082:18256591:18256686:18258183:1825826218256591:18256686ENSG00000124795.10ENST00000505224.1,ENST00000397239.3,ENST00000503715.1,ENST00000244776.7
exon_skip_456554618256603:18256686:18258183:18258293:18258534:1825863618258183:18258293ENSG00000124795.10ENST00000397239.3,ENST00000503715.1,ENST00000515742.1
exon_skip_456557618258183:18258293:18258534:18258636:18264073:1826422718258534:18258636ENSG00000124795.10ENST00000397239.3,ENST00000515742.1
exon_skip_456564618258587:18258636:18264073:18264227:18264615:1826476618264073:18264227ENSG00000124795.10ENST00000505224.1

check button PSI values of skipped exons in TCGA.
psi tcga

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Exon skipping events with PSIs in GTEx for DEK

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_456531618225841:18225961:18226404:18226473:18236682:1823682718226404:18226473ENSG00000124795.10ENST00000397239.3,ENST00000505224.1,ENST00000244776.7
exon_skip_456539618226404:18226473:18236682:18236831:18237611:1823774718236682:18236831ENSG00000124795.10ENST00000397239.3,ENST00000505224.1,ENST00000244776.7,ENST00000507591.1
exon_skip_456542618237611:18237747:18244738:18244834:18249881:1824991018244738:18244834ENSG00000124795.10ENST00000515770.1
exon_skip_456543618237611:18237747:18249881:18250070:18255961:1825608118249881:18250070ENSG00000124795.10ENST00000397239.3,ENST00000505224.1,ENST00000244776.7,ENST00000512145.1
exon_skip_456545618249881:18250070:18255961:18256082:18256591:1825660518255961:18256082ENSG00000124795.10ENST00000397239.3,ENST00000505224.1,ENST00000244776.7,ENST00000515770.1,ENST00000512145.1
exon_skip_456552618255966:18256082:18256591:18256686:18258183:1825826218256591:18256686ENSG00000124795.10ENST00000397239.3,ENST00000505224.1,ENST00000244776.7,ENST00000503715.1
exon_skip_456554618256603:18256686:18258183:18258293:18258534:1825863618258183:18258293ENSG00000124795.10ENST00000397239.3,ENST00000503715.1,ENST00000515742.1
exon_skip_456557618258183:18258293:18258534:18258636:18264073:1826422718258534:18258636ENSG00000124795.10ENST00000397239.3,ENST00000515742.1
exon_skip_456564618258587:18258636:18264073:18264227:18264615:1826476618264073:18264227ENSG00000124795.10ENST00000505224.1

check button PSI values of skipped exons in GTEx.
psi gtex

* Skipped exon sequences.

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

check button Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000003972391823668218236831Frame-shift
ENST000003972391825596118256082Frame-shift
ENST000003972391825659118256686Frame-shift
ENST000003972391825818318258293Frame-shift
ENST000003972391822640418226473In-frame
ENST000003972391824988118250070In-frame
ENST000003972391825853418258636In-frame

check button Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000003972391823668218236831Frame-shift
ENST000003972391825596118256082Frame-shift
ENST000003972391825659118256686Frame-shift
ENST000003972391825818318258293Frame-shift
ENST000003972391822640418226473In-frame
ENST000003972391824988118250070In-frame
ENST000003972391825853418258636In-frame

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

check button Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.
prot feature distribution

check button Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST00000397239344437518258534182586365946954882
ENST000003972393444375182498811825007010221210191254
ENST000003972393444375182264041822647314961564349372

check button Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST00000397239344437518258534182586365946954882
ENST000003972393444375182498811825007010221210191254
ENST000003972393444375182264041822647314961564349372

check button Lost protein functional features of individual exon skipping events in TCGA.
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
P3565948824982Alternative sequenceID=VSP_042951;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
P3565948822375ChainID=PRO_0000079858;Note=Protein DEK
P3565948823049Compositional biasNote=Asp/Glu-rich (highly acidic)
P3565948825151Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:21406692,ECO:0000244|PubMed:23186163;Dbxref=PMID:17081983,PMID:20068231,PMID:21406692,PMID
P3565948827272Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:23186163;Dbxref=PMID:23186163
P356591912542375ChainID=PRO_0000079858;Note=Protein DEK
P35659191254228236Compositional biasNote=Asp/Glu-rich (acidic)
P35659191254241254Compositional biasNote=Asp/Glu-rich (acidic)
P35659191254199199Modified residueNote=Phosphothreonine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254201201Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254204204Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254210210Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:20068231;Dbxref=PMID:20068231
P35659191254227227Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:17081983;Dbxref=PMID:17081983
P35659191254230230Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254231231Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254232232Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254243243Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254244244Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254251251Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254205221MotifNote=Nuclear localization signal;Ontology_term=ECO:0000255;evidence=ECO:0000255
P35659349372355357Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V
P356593493722375ChainID=PRO_0000079858;Note=Protein DEK
P35659349372337351DNA binding.
P35659349372367371DNA binding.
P35659349372343353HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V
P35659349372361375HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V


check button Lost protein functional features of individual exon skipping events in GTEx.
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
P3565948824982Alternative sequenceID=VSP_042951;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
P3565948822375ChainID=PRO_0000079858;Note=Protein DEK
P3565948823049Compositional biasNote=Asp/Glu-rich (highly acidic)
P3565948825151Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:21406692,ECO:0000244|PubMed:23186163;Dbxref=PMID:17081983,PMID:20068231,PMID:21406692,PMID
P3565948827272Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:23186163;Dbxref=PMID:23186163
P356591912542375ChainID=PRO_0000079858;Note=Protein DEK
P35659191254228236Compositional biasNote=Asp/Glu-rich (acidic)
P35659191254241254Compositional biasNote=Asp/Glu-rich (acidic)
P35659191254199199Modified residueNote=Phosphothreonine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254201201Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254204204Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254210210Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:20068231;Dbxref=PMID:20068231
P35659191254227227Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:17081983;Dbxref=PMID:17081983
P35659191254230230Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254231231Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254232232Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:17081983,ECO:0000244|PubMed:20068231,ECO:0000244|PubMed:24275569;Dbxref=PMID:17081983,PMID:20068231,PMID:24275569
P35659191254243243Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254244244Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254251251Modified residueNote=Phosphoserine%3B by CK2;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:15199154;Dbxref=PMID:15199154
P35659191254205221MotifNote=Nuclear localization signal;Ontology_term=ECO:0000255;evidence=ECO:0000255
P35659349372355357Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V
P356593493722375ChainID=PRO_0000079858;Note=Protein DEK
P35659349372337351DNA binding.
P35659349372367371DNA binding.
P35659349372343353HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V
P35659349372361375HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:1Q1V


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SNVs in the skipped exons for DEK

check button - Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.
lollipop

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

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-G3-A3CJ-01exon_skip_456531
18226405182264731822641918226419Frame_Shift_DelT-p.T369fs
PAADTCGA-IB-7654-01exon_skip_456539
18236683182368311823673718236740Frame_Shift_DelTTTC-p.KK330fs
LIHCTCGA-DD-A1EG-01exon_skip_456543
18249882182500701824992818249928Frame_Shift_DelT-p.N239fs
LIHCTCGA-DD-A39Y-01exon_skip_456543
18249882182500701824992818249928Frame_Shift_DelT-p.N239fs
LIHCTCGA-G3-A3CJ-01exon_skip_456543
18249882182500701824992818249928Frame_Shift_DelT-p.N239fs
LIHCTCGA-DD-A39Y-01exon_skip_456543
18249882182500701824993418249934Frame_Shift_DelT-p.K238fs
LIHCTCGA-DD-A3A0-01exon_skip_456543
18249882182500701824993418249934Frame_Shift_DelT-p.K238fs
LIHCTCGA-G3-A3CJ-01exon_skip_456543
18249882182500701824993418249934Frame_Shift_DelT-p.K238fs
LIHCTCGA-DD-A3A0-01exon_skip_456543
18249882182500701825002718250027Frame_Shift_DelT-p.K206fs
LIHCTCGA-DD-A1EG-01exon_skip_456543
18249882182500701825004918250049Frame_Shift_DelT-p.T199fs
LIHCTCGA-DD-A39Y-01exon_skip_456543
18249882182500701825004918250049Frame_Shift_DelT-p.T199fs
COADTCGA-AY-6197-01exon_skip_456552
18256592182566861825663318256633Frame_Shift_DelT-p.G138fs
LIHCTCGA-DD-A3A0-01exon_skip_456552
18256592182566861825663318256633Frame_Shift_DelT-p.K137fs
LIHCTCGA-G3-A3CJ-01exon_skip_456557
18258535182586361825858718258587Frame_Shift_DelC-p.R65fs
LIHCTCGA-DD-A39Y-01exon_skip_456557
18258535182586361825859618258596Frame_Shift_DelT-p.K62fs
HNSCTCGA-F7-A624-01exon_skip_456564
18264074182642271826418818264188Frame_Shift_DelC-p.E11fs
STADTCGA-CG-5723-01exon_skip_456557
18258535182586361825859518258596Frame_Shift_Ins-Tp.V63fs
STADTCGA-CG-5723-01exon_skip_456557
18258535182586361825859618258597Frame_Shift_Ins-Tp.K62fs
UCECTCGA-AX-A05Z-01exon_skip_456552
18256592182566861825663218256632Nonsense_MutationCAp.G138*

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
HCT116_LARGE_INTESTINE18258184182582931825825018258250Frame_Shift_DelA-p.F97fs
SNU407_LARGE_INTESTINE18258184182582931825825018258250Frame_Shift_DelA-p.F97fs
CW2_LARGE_INTESTINE18249882182500701825004818250049Frame_Shift_Ins-Tp.T199fs
NCIH250_LUNG18226405182264731822643618226436Missense_MutationCTp.R362K
JHUEM1_ENDOMETRIUM18226405182264731822646118226461Missense_MutationAGp.Y354H
HEC251_ENDOMETRIUM18236683182368311823674018236740Missense_MutationCAp.K330N
NCIH661_LUNG18236683182368311823678018236780Missense_MutationTCp.K317R
HCT15_LARGE_INTESTINE18255962182560821825602918256029Missense_MutationGAp.S169L
SC1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE18256592182566861825663618256636Missense_MutationTAp.E136D
SCI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE18256592182566861825663618256636Missense_MutationTAp.E136D
HCC2450_LUNG18258184182582931825822118258221Missense_MutationCGp.R107T
COLO794_SKIN18264074182642271826409918264099Missense_MutationGCp.D40E
COLO800_SKIN18264074182642271826409918264099Missense_MutationGCp.D40E
COLO818_SKIN18264074182642271826409918264099Missense_MutationGCp.D40E
OVCA420_OVARY18264074182642271826410318264103Missense_MutationTCp.D39G
WM1799_SKIN18264074182642271826412118264121Missense_MutationTCp.E33G
KYSE270_OESOPHAGUS18264074182642271826416318264163Missense_MutationGAp.S19F
HPAFII_PANCREAS18264074182642271826420018264200Missense_MutationCTp.A7T
PCI6A_UPPER_AERODIGESTIVE_TRACT18249882182500701824996418249964Nonsense_MutationGCp.S227*
HCT15_LARGE_INTESTINE18256592182566861825663218256632Nonsense_MutationCAp.G138*
SNU324_PANCREAS18236683182368311823668418236684Splice_SiteT-p.K349fs
BICR18_UPPER_AERODIGESTIVE_TRACT18255962182560821825607818256084Splice_SiteTAAATCT-p.KDL151fs
HS611T_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE18256592182566861825668618256686Splice_SiteCTp.V120M
HCC2450_LUNG18258184182582931825829318258293Splice_SiteCGp.G83A
COLO783_SKIN18264074182642271826421618264216Start_Codon_SNPCTp.M1I

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

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for DEK


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for DEK


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RelatedDrugs for DEK

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

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RelatedDiseases for DEK

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
DEKC0027626Neoplasm Invasiveness1CTD_human