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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 CTNND1

check button Gene summary
Gene informationGene symbol

CTNND1

Gene ID

1500

Gene namecatenin delta 1
SynonymsBCDS2|CAS|CTNND|P120CAS|P120CTN|p120|p120(CAS)|p120(CTN)
Cytomap

11q12.1

Type of geneprotein-coding
Descriptioncatenin delta-1cadherin-associated Src substratecatenin (cadherin-associated protein), delta 1p120 catenin
Modification date20180523
UniProtAcc

O60716

ContextPubMed: CTNND1 [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 CTNND1 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 CTNND1

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 CTNND1

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_594461157529268:57529518:57556508:57556627:57558856:5755914557556508:57556627ENSG00000198561.8ENST00000358694.6
exon_skip_594471157529268:57529518:57556508:57556627:57558965:5755914557556508:57556627ENSG00000198561.8ENST00000532649.1
exon_skip_594491157529268:57529518:57558856:57559145:57561481:5756155357558856:57559145ENSG00000198561.8ENST00000428599.2,ENST00000526938.1
exon_skip_594511157529268:57529518:57558965:57559145:57561481:5756155357558965:57559145ENSG00000198561.8ENST00000530748.1,ENST00000529873.1,ENST00000528621.1,ENST00000526357.1,ENST00000532844.1
exon_skip_594531157529268:57529518:57561481:57561553:57563048:5756320157561481:57561553ENSG00000198561.8ENST00000532787.1,ENST00000528232.1,ENST00000530094.1,ENST00000415361.2,ENST00000529986.1
exon_skip_594561157571092:57571276:57572134:57572252:57573353:5757350757572134:57572252ENSG00000198561.8ENST00000532787.1,ENST00000361796.4,ENST00000525902.1,ENST00000529526.1,ENST00000358694.6,ENST00000530748.1,ENST00000428599.2,ENST00000426142.2,ENST00000361332.4,ENST00000528232.1,ENST00000399050.4,ENST00000534579.1,ENST00000533667.1,ENST00000532463.1,ENS
exon_skip_594571157573360:57573507:57573932:57573950:57574386:5757445557573932:57573950ENSG00000198561.8ENST00000525902.1,ENST00000530748.1,ENST00000528232.1,ENST00000399050.4,ENST00000399039.4,ENST00000526938.1,ENST00000527467.1,ENST00000360682.6,ENST00000415361.2,ENST00000529919.1,ENST00000532844.1
exon_skip_594591157576745:57576938:57577580:57577695:57578870:5757895857577580:57577695ENSG00000198561.8ENST00000532787.1,ENST00000361796.4,ENST00000525902.1,ENST00000529526.1,ENST00000358694.6,ENST00000530748.1,ENST00000428599.2,ENST00000426142.2,ENST00000361332.4,ENST00000528232.1,ENST00000399050.4,ENST00000534579.1,ENST00000533667.1,ENST00000532463.1,ENS
exon_skip_594651157577616:57577695:57578870:57578958:57581782:5758184557578870:57578958ENSG00000198561.8ENST00000361796.4,ENST00000525902.1,ENST00000529526.1,ENST00000358694.6,ENST00000530748.1,ENST00000428599.2,ENST00000426142.2,ENST00000361332.4,ENST00000528232.1,ENST00000399050.4,ENST00000534579.1,ENST00000532463.1,ENST00000399039.4,ENST00000530094.1,ENS
exon_skip_594661157577616:57577695:57578870:57578958:57582865:5758295357578870:57578958ENSG00000198561.8ENST00000532787.1,ENST00000533667.1,ENST00000529873.1,ENST00000361391.6,ENST00000526938.1,ENST00000360682.6
exon_skip_594691157578870:57578958:57581782:57581845:57582865:5758295357581782:57581845ENSG00000198561.8ENST00000361796.4,ENST00000525902.1,ENST00000529526.1,ENST00000358694.6,ENST00000530748.1,ENST00000428599.2,ENST00000426142.2,ENST00000361332.4,ENST00000528232.1,ENST00000399050.4,ENST00000534579.1,ENST00000532463.1,ENST00000399039.4,ENST00000530094.1,ENS
exon_skip_594701157581782:57581845:57582865:57582972:57583386:5758347357582865:57582972ENSG00000198561.8ENST00000361332.4,ENST00000399050.4,ENST00000530094.1,ENST00000527467.1,ENST00000415361.2,ENST00000526357.1,ENST00000532844.1,ENST00000531014.1
exon_skip_594721157581782:57581845:57582865:57582972:57583768:5758418957582865:57582972ENSG00000198561.8ENST00000361796.4,ENST00000525902.1,ENST00000529526.1,ENST00000358694.6,ENST00000530748.1,ENST00000428599.2,ENST00000426142.2,ENST00000528232.1,ENST00000534579.1,ENST00000532463.1,ENST00000526772.1,ENST00000532649.1,ENST00000528621.1,ENST00000524630.1,ENS
exon_skip_594761157582865:57582972:57583386:57583473:57583768:5758418957583386:57583473ENSG00000198561.8ENST00000532787.1,ENST00000361332.4,ENST00000399050.4,ENST00000533667.1,ENST00000530094.1,ENST00000529873.1,ENST00000361391.6,ENST00000527467.1,ENST00000360682.6,ENST00000415361.2,ENST00000526357.1,ENST00000532844.1,ENST00000531014.1

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

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Exon skipping events with PSIs in GTEx for CTNND1

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_594461157529268:57529518:57556508:57556627:57558856:5755914557556508:57556627ENSG00000198561.8ENST00000358694.6
exon_skip_594471157529268:57529518:57556508:57556627:57558965:5755914557556508:57556627ENSG00000198561.8ENST00000532649.1
exon_skip_594491157529268:57529518:57558856:57559145:57561481:5756155357558856:57559145ENSG00000198561.8ENST00000428599.2,ENST00000526938.1
exon_skip_594511157529268:57529518:57558965:57559145:57561481:5756155357558965:57559145ENSG00000198561.8ENST00000528621.1,ENST00000530748.1,ENST00000529873.1,ENST00000532844.1,ENST00000526357.1
exon_skip_594531157529268:57529518:57561481:57561553:57563048:5756320157561481:57561553ENSG00000198561.8ENST00000529986.1,ENST00000532787.1,ENST00000528232.1,ENST00000530094.1,ENST00000415361.2
exon_skip_594561157571092:57571276:57572134:57572252:57573353:5757350757572134:57572252ENSG00000198561.8ENST00000524630.1,ENST00000529919.1,ENST00000399039.4,ENST00000360682.6,ENST00000361796.4,ENST00000529526.1,ENST00000426142.2,ENST00000399050.4,ENST00000361391.6,ENST00000361332.4,ENST00000532463.1,ENST00000529986.1,ENST00000358694.6,ENST00000532787.1,ENS
exon_skip_594571157573360:57573507:57573932:57573950:57574386:5757445557573932:57573950ENSG00000198561.8ENST00000529919.1,ENST00000399039.4,ENST00000360682.6,ENST00000399050.4,ENST00000530748.1,ENST00000527467.1,ENST00000528232.1,ENST00000525902.1,ENST00000532844.1,ENST00000415361.2,ENST00000526938.1
exon_skip_594591157576745:57576938:57577580:57577695:57578870:5757895857577580:57577695ENSG00000198561.8ENST00000524630.1,ENST00000529919.1,ENST00000399039.4,ENST00000360682.6,ENST00000361796.4,ENST00000529526.1,ENST00000426142.2,ENST00000399050.4,ENST00000361391.6,ENST00000361332.4,ENST00000532463.1,ENST00000529986.1,ENST00000358694.6,ENST00000532787.1,ENS
exon_skip_594651157577616:57577695:57578870:57578958:57581782:5758184557578870:57578958ENSG00000198561.8ENST00000524630.1,ENST00000529919.1,ENST00000399039.4,ENST00000361796.4,ENST00000529526.1,ENST00000426142.2,ENST00000399050.4,ENST00000361332.4,ENST00000532463.1,ENST00000529986.1,ENST00000358694.6,ENST00000532649.1,ENST00000528621.1,ENST00000530748.1,ENS
exon_skip_594661157577616:57577695:57578870:57578958:57582865:5758295357578870:57578958ENSG00000198561.8ENST00000360682.6,ENST00000361391.6,ENST00000532787.1,ENST00000533667.1,ENST00000529873.1,ENST00000526938.1
exon_skip_594691157578870:57578958:57581782:57581845:57582865:5758295357581782:57581845ENSG00000198561.8ENST00000524630.1,ENST00000529919.1,ENST00000399039.4,ENST00000361796.4,ENST00000529526.1,ENST00000426142.2,ENST00000399050.4,ENST00000361332.4,ENST00000532463.1,ENST00000529986.1,ENST00000358694.6,ENST00000532649.1,ENST00000528621.1,ENST00000530748.1,ENS
exon_skip_594701157581782:57581845:57582865:57582972:57583386:5758347357582865:57582972ENSG00000198561.8ENST00000399050.4,ENST00000361332.4,ENST00000527467.1,ENST00000531014.1,ENST00000532844.1,ENST00000526357.1,ENST00000530094.1,ENST00000415361.2
exon_skip_594721157581782:57581845:57582865:57582972:57583768:5758418957582865:57582972ENSG00000198561.8ENST00000524630.1,ENST00000361796.4,ENST00000529526.1,ENST00000426142.2,ENST00000532463.1,ENST00000529986.1,ENST00000358694.6,ENST00000532649.1,ENST00000528621.1,ENST00000530748.1,ENST00000428599.2,ENST00000528232.1,ENST00000526772.1,ENST00000525902.1,ENS
exon_skip_594761157582865:57582972:57583386:57583473:57583768:5758418957583386:57583473ENSG00000198561.8ENST00000360682.6,ENST00000399050.4,ENST00000361391.6,ENST00000361332.4,ENST00000532787.1,ENST00000533667.1,ENST00000527467.1,ENST00000531014.1,ENST00000529873.1,ENST00000532844.1,ENST00000526357.1,ENST00000530094.1,ENST00000415361.2

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 CTNND1

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
ENST000003990505757213457572252Frame-shift
ENST000003990505757758057577695Frame-shift
ENST000003990505757887057578958Frame-shift
ENST000003990505758286557582972Frame-shift
ENST000003990505757393257573950In-frame
ENST000003990505758178257581845In-frame
ENST000003990505758338657583473In-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
ENST000003990505757213457572252Frame-shift
ENST000003990505757758057577695Frame-shift
ENST000003990505757887057578958Frame-shift
ENST000003990505758286557582972Frame-shift
ENST000003990505757393257573950In-frame
ENST000003990505758178257581845In-frame
ENST000003990505758338657583473In-frame

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Infer the effects of exon skipping event on protein functional features for CTNND1

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
ENST000003990506330968575817825758184531753237879900
ENST000003990506330968575833865758347333453431936965

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
ENST000003990506330968575817825758184531753237879900
ENST000003990506330968575833865758347333453431936965

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


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


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SNVs in the skipped exons for CTNND1

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.
CTNND1_LIHC_exon_skip_59476_psi_boxplot.png
boxplot

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
STADTCGA-CG-5733-01exon_skip_59449
57558857575591455755899257558993Frame_Shift_DelCT-p.A14fs
STADTCGA-CG-5733-01exon_skip_59451
57558966575591455755899257558993Frame_Shift_DelCT-p.A14fs
COADTCGA-AA-3713-01exon_skip_59459
57577581575776955757766457577664Frame_Shift_DelA-p.E780fs
STADTCGA-BR-8284-01exon_skip_59459
57577581575776955757766457577664Frame_Shift_DelA-p.E840fs
LIHCTCGA-DD-A39Y-01exon_skip_59466
exon_skip_59465
57578871575789585757895057578950Frame_Shift_DelA-p.Q871fs
PAADTCGA-2J-AABK-01exon_skip_59472
exon_skip_59470
57582866575829725758292057582920Frame_Shift_DelG-p.R913fs
PAADTCGA-2J-AABK-01exon_skip_59472
exon_skip_59470
57582866575829725758292057582920Frame_Shift_DelG-p.R919fs
LIHCTCGA-G3-A3CJ-01exon_skip_59476
57583387575834735758343357583433Frame_Shift_DelT-p.V952fs
LIHCTCGA-DD-A1EG-01exon_skip_59476
57583387575834735758344657583446Frame_Shift_DelG-p.E956fs
UCECTCGA-DI-A1NN-01exon_skip_59456
57572135575722525757217057572171Frame_Shift_Ins-ACTTp.K547fs
UCECTCGA-DI-A1NN-01exon_skip_59456
57572135575722525757217057572171Frame_Shift_Ins-ACTTp.R549fs
STADTCGA-BR-7851-01exon_skip_59466
exon_skip_59465
57578871575789585757894957578950Frame_Shift_Ins-Ap.Q877fs
STADTCGA-BR-7851-01exon_skip_59466
exon_skip_59465
57578871575789585757895057578951Frame_Shift_Ins-Ap.Q877fs
COADTCGA-A6-5665-01exon_skip_59469
57581783575818455758182557581826Frame_Shift_Ins-Ap.G834fs
READTCGA-EI-6917-01exon_skip_59459
57577581575776955757760357577603Nonsense_MutationCTp.R814X
SKCMTCGA-EE-A2MS-06exon_skip_59459
57577581575776955757760357577603Nonsense_MutationCTp.R814*
SKCMTCGA-EE-A2MS-06exon_skip_59459
57577581575776955757760357577603Nonsense_MutationCTp.R814X
STADTCGA-D7-A4Z0-01exon_skip_59459
57577581575776955757760357577603Nonsense_MutationCTp.R820*
UCECTCGA-BS-A0UA-01exon_skip_59459
57577581575776955757760357577603Nonsense_MutationCTp.R820*
LIHCTCGA-FV-A496-01exon_skip_59459
57577581575776955757763657577636Nonsense_MutationGTp.G825*
LIHCTCGA-FV-A496-01exon_skip_59459
57577581575776955757763657577636Nonsense_MutationGTp.G831X
UCECTCGA-D1-A17Q-01exon_skip_59459
57577581575776955757766957577669Nonsense_MutationGTp.E842*
UCECTCGA-AP-A056-01exon_skip_59453
57561482575615535756155457561554Splice_SiteGAe2+1
HNSCTCGA-CR-7367-01exon_skip_59472
exon_skip_59470
57582866575829725758297457582974Splice_SiteTCp.M936_splice

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
CTNND1_57582865_57582972_57583386_57583473_57583768_57584189_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_59476
Skipped exon start: 57583387
Skipped exon end: 57583473
Mutation start: 57583446
Mutation end: 57583446
Mutation type: Frame_Shift_Del
Reference seq: G
Mutation seq: -
AAchange: p.E956fs
exon_skip_103075_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_100809_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_101656_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_10700_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_109033_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_110000_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_110381_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_110545_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_11218_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_11256_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_11259_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_11263_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_115462_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_115587_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_116330_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_121002_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_123667_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_12440_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_125045_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_129202_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_129996_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_130099_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_13071_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_131505_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_131697_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_133542_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_133548_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_134792_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_135418_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_135741_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_135763_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_135820_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_13608_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_138255_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_138373_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_138947_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_140996_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_141914_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_143553_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_143841_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_143843_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_144075_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_144116_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_144125_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_146762_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_146776_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_146807_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_14772_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_148738_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_148740_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_14897_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_14899_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_15042_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_150985_LIHC_TCGA-DD-A1EG-01.png
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exon_skip_153494_LIHC_TCGA-DD-A1EG-01.png
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CTNND1_57582865_57582972_57583386_57583473_57583768_57584189_TCGA-G3-A3CJ-01Sample: TCGA-G3-A3CJ-01
Cancer type: LIHC
ESID: exon_skip_59476
Skipped exon start: 57583387
Skipped exon end: 57583473
Mutation start: 57583433
Mutation end: 57583433
Mutation type: Frame_Shift_Del
Reference seq: T
Mutation seq: -
AAchange: p.V952fs
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check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SKOV3_OVARY57558857575591455755900857559008Missense_MutationGAp.E20K
SKOV3_OVARY57558966575591455755900857559008Missense_MutationGAp.E20K
HCC2998_LARGE_INTESTINE57558857575591455755909757559097Missense_MutationACp.Q49H
HCC2998_LARGE_INTESTINE57558966575591455755909757559097Missense_MutationACp.Q49H
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57558857575591455755913557559135Missense_MutationGAp.R62H
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57558966575591455755913557559135Missense_MutationGAp.R62H
GP2D_LARGE_INTESTINE57572135575722525757215657572156Missense_MutationTAp.S542R
JHUEM1_ENDOMETRIUM57572135575722525757216657572166Missense_MutationCTp.R546W
HCC2998_LARGE_INTESTINE57572135575722525757217557572175Missense_MutationCTp.R549W
NCIH1435_LUNG57577581575776955757760457577604Missense_MutationGTp.R820L
NCIH23_LUNG57577581575776955757763657577636Missense_MutationGAp.G831R
NALM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57577581575776955757765257577652Missense_MutationGAp.R836Q
CL40_LARGE_INTESTINE57578871575789585757889357578893Missense_MutationGAp.R858Q
CAL78_BONE57581783575818455758178757581787Missense_MutationGTp.K881N
NCIH650_LUNG57582866575829725758287157582871Missense_MutationATp.N903Y
PFSK1_CENTRAL_NERVOUS_SYSTEM57582866575829725758290557582905Missense_MutationAGp.N914S
SW756_CERVIX57582866575829725758293157582931Missense_MutationCGp.L923V
HSC1_SKIN57582866575829725758297057582970Missense_MutationACp.M936L
PK45H_PANCREAS57582866575829725758297057582970Missense_MutationACp.M936L
HEC265_ENDOMETRIUM57582866575829725758297057582970Missense_MutationACp.M936L
MOLM16_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57582866575829725758297057582970Missense_MutationACp.M936L
MOLP8_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57582866575829725758297057582970Missense_MutationACp.M936L
RKN_SOFT_TISSUE57582866575829725758297057582970Missense_MutationACp.M936L
TEN_ENDOMETRIUM57582866575829725758297057582970Missense_MutationACp.M936L
NUGC3_STOMACH57582866575829725758297057582970Missense_MutationACp.M936L
OSRC2_KIDNEY57582866575829725758297057582970Missense_MutationACp.M936L
SUIT2_PANCREAS57582866575829725758297057582970Missense_MutationACp.M936L
MMACSF_SKIN57582866575829725758297057582970Missense_MutationACp.M936L
OC316_OVARY57583387575834735758344757583447Missense_MutationGTp.G957W
OC314_OVARY57583387575834735758344757583447Missense_MutationGTp.G957W
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE57583387575834735758345057583451Missense_MutationGGAAp.G958N
C99_LARGE_INTESTINE57577581575776955757760357577603Nonsense_MutationCTp.R820*
HT115_LARGE_INTESTINE57577581575776955757760357577603Nonsense_MutationCTp.R820*
SNU478_BILIARY_TRACT57577581575776955757768157577681Nonsense_MutationATp.K846*
SUIT2_PANCREAS57578871575789585757894957578949Nonsense_MutationCTp.Q877*
SW48_LARGE_INTESTINE57573933575739505757393357573933Splice_SiteAGp.D626G
LS411N_LARGE_INTESTINE57577581575776955757769457577694Splice_SiteAGp.Q850R

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for CTNND1

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 CTNND1


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for CTNND1


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RelatedDrugs for CTNND1

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 CTNND1

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