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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 ST5

check button Gene summary
Gene informationGene symbol

ST5

Gene ID

6764

Gene namesuppression of tumorigenicity 5
SynonymsDENND2B|HTS1|p126
Cytomap

11p15.4

Type of geneprotein-coding
Descriptionsuppression of tumorigenicity 5 proteinDENN/MADD domain containing 2BheLa tumor suppression 1
Modification date20180519
UniProtAcc

P78524

ContextPubMed: ST5 [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 ST5 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 ST5

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 ST5

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_68666118717009:8717096:8717973:8718213:8719071:87191838717973:8718213ENSG00000166444.13ENST00000532162.1,ENST00000526099.1,ENST00000534127.1,ENST00000534278.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1
exon_skip_68668118719122:8719183:8720479:8720521:8720759:87209378720479:8720521ENSG00000166444.13ENST00000526099.1,ENST00000532871.1,ENST00000534127.1,ENST00000534278.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526062.1,ENST00000530438.1
exon_skip_68682118720479:8720521:8720759:8720937:8724118:87242048720759:8720937ENSG00000166444.13ENST00000526099.1,ENST00000534127.1,ENST00000534278.1,ENST00000533081.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1
exon_skip_68683118720479:8720521:8720759:8720937:8728631:87287728720759:8720937ENSG00000166444.13ENST00000532871.1
exon_skip_68711118720759:8720937:8721403:8721559:8724118:87242048721403:8721559ENSG00000166444.13ENST00000526062.1
exon_skip_68713118720759:8720937:8724118:8724267:8728631:87287728724118:8724267ENSG00000166444.13ENST00000526099.1,ENST00000534127.1,ENST00000534278.1,ENST00000533081.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1
exon_skip_68737118728752:8728772:8729323:8729401:8732391:87324578729323:8729401ENSG00000166444.13ENST00000530338.1,ENST00000532734.1,ENST00000526099.1,ENST00000526701.1,ENST00000534127.1,ENST00000526837.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68746118732391:8732461:8732668:8732778:8734097:87342678732668:8732778ENSG00000166444.13ENST00000526099.1,ENST00000534127.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68749118732672:8732778:8733450:8733583:8734097:87342678733450:8733583ENSG00000166444.13ENST00000532734.1
exon_skip_68750118732672:8732778:8734097:8734282:8735544:87355898734097:8734282ENSG00000166444.13ENST00000526099.1,ENST00000534127.1,ENST00000526757.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68753118734146:8734282:8735544:8735589:8736156:87362538735544:8735589ENSG00000166444.13ENST00000532734.1,ENST00000526099.1,ENST00000534127.1,ENST00000526757.1,ENST00000528527.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68754118736156:8736253:8737149:8737365:8739287:87393838737149:8737365ENSG00000166444.13ENST00000532734.1,ENST00000526099.1,ENST00000530593.1,ENST00000534127.1,ENST00000526757.1,ENST00000528527.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68761118739428:8739439:8747619:8747756:8751496:87527568747619:8747756ENSG00000166444.13ENST00000534127.1,ENST00000313726.6,ENST00000357665.1
exon_skip_68762118739428:8739439:8747619:8747756:8772167:87722728747619:8747756ENSG00000166444.13ENST00000530580.1,ENST00000532734.1,ENST00000528196.1,ENST00000531093.1,ENST00000533225.1,ENST00000526757.1,ENST00000527510.1,ENST00000533425.1,ENST00000530438.1
exon_skip_68763118739428:8739439:8747619:8747756:8832063:88321968747619:8747756ENSG00000166444.13ENST00000528527.1
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENSG00000166444.13ENST00000534127.1,ENST00000313726.6,ENST00000357665.1
exon_skip_68771118747619:8747756:8772167:8772272:8832063:88321968772167:8772272ENSG00000166444.13ENST00000527510.1,ENST00000533425.1,ENST00000530438.1
exon_skip_68773118747619:8747756:8772167:8772272:8832793:88328828772167:8772272ENSG00000166444.13ENST00000533225.1,ENST00000526126.1
exon_skip_68779118772167:8772272:8832793:8832882:8853102:88532358832793:8832882ENSG00000166444.13ENST00000527392.1,ENST00000525169.1,ENST00000533225.1,ENST00000526126.1,ENST00000526828.1,ENST00000530959.1
exon_skip_68780118772167:8772272:8832793:8832882:8860856:88608978832793:8832882ENSG00000166444.13ENST00000534665.1,ENST00000524757.1,ENST00000534127.1,ENST00000527347.1,ENST00000357665.1,ENST00000527516.1
exon_skip_68782118772167:8772272:8832793:8832882:8892500:88925318832793:8832882ENSG00000166444.13ENST00000533471.1,ENST00000526155.1
exon_skip_68784118772167:8772272:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000530938.1
exon_skip_68791118772167:8772272:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000526241.1
exon_skip_68794118832829:8832878:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000531640.1
exon_skip_68799118832793:8832882:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000525169.1,ENST00000526126.1,ENST00000532651.1
exon_skip_68801118832793:8832882:8853102:8853235:8892500:88925318853102:8853235ENSG00000166444.13ENST00000527392.1
exon_skip_68807118832793:8832882:8860856:8860897:8892381:88924648860856:8860897ENSG00000166444.13ENST00000527347.1
exon_skip_68808118832793:8832882:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000534665.1,ENST00000527516.1
exon_skip_68810118832793:8832882:8860856:8860897:8902556:89026568860856:8860897ENSG00000166444.13ENST00000534127.1
exon_skip_68814118832793:8832882:8892500:8892635:8892880:88929148892500:8892635ENSG00000166444.13ENST00000533471.1
exon_skip_68819118853102:8853235:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000530938.1,ENST00000525169.1,ENST00000526126.1
exon_skip_68820118853102:8853235:8860856:8860897:8892880:88929148860856:8860897ENSG00000166444.13ENST00000532651.1
exon_skip_68821118853102:8853235:8892500:8892635:8892880:88929148892500:8892635ENSG00000166444.13ENST00000527392.1
exon_skip_68823118860856:8860897:8878889:8878983:8892500:88926358878889:8878983ENSG00000166444.13ENST00000524757.1
exon_skip_68824118860856:8860897:8892500:8892635:8892880:88929148892500:8892635ENSG00000166444.13ENST00000525169.1,ENST00000527516.1

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

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Exon skipping events with PSIs in GTEx for ST5

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_68666118717009:8717096:8717973:8718213:8719071:87191838717973:8718213ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000532162.1,ENST00000534278.1,ENST00000530438.1
exon_skip_68668118719122:8719183:8720479:8720521:8720759:87209378720479:8720521ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000534278.1,ENST00000530438.1,ENST00000526062.1,ENST00000532871.1
exon_skip_68682118720479:8720521:8720759:8720937:8724118:87242048720759:8720937ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000534278.1,ENST00000530438.1,ENST00000533081.1
exon_skip_68683118720479:8720521:8720759:8720937:8728631:87287728720759:8720937ENSG00000166444.13ENST00000532871.1
exon_skip_68711118720759:8720937:8721403:8721559:8724118:87242048721403:8721559ENSG00000166444.13ENST00000526062.1
exon_skip_68713118720759:8720937:8724118:8724267:8728631:87287728724118:8724267ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000534278.1,ENST00000530438.1,ENST00000533081.1
exon_skip_68737118728752:8728772:8729323:8729401:8732391:87324578729323:8729401ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000530438.1,ENST00000526701.1,ENST00000533020.1,ENST00000526837.1,ENST00000530338.1,ENST00000532734.1
exon_skip_68746118732391:8732461:8732668:8732778:8734097:87342678732668:8732778ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68749118732672:8732778:8733450:8733583:8734097:87342678733450:8733583ENSG00000166444.13ENST00000532734.1
exon_skip_68750118732672:8732778:8734097:8734282:8735544:87355898734097:8734282ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000530438.1,ENST00000533020.1
exon_skip_68753118734146:8734282:8735544:8735589:8736156:87362538735544:8735589ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000530438.1,ENST00000533020.1,ENST00000532734.1,ENST00000528527.1
exon_skip_68754118736156:8736253:8737149:8737365:8739287:87393838737149:8737365ENSG00000166444.13ENST00000526757.1,ENST00000534127.1,ENST00000313726.6,ENST00000530991.1,ENST00000357665.1,ENST00000526099.1,ENST00000530438.1,ENST00000533020.1,ENST00000532734.1,ENST00000530593.1,ENST00000528527.1
exon_skip_68761118739428:8739439:8747619:8747756:8751496:87527568747619:8747756ENSG00000166444.13ENST00000534127.1,ENST00000313726.6,ENST00000357665.1
exon_skip_68762118739428:8739439:8747619:8747756:8772167:87722728747619:8747756ENSG00000166444.13ENST00000526757.1,ENST00000530438.1,ENST00000532734.1,ENST00000533425.1,ENST00000528196.1,ENST00000527510.1,ENST00000530580.1,ENST00000531093.1,ENST00000533225.1
exon_skip_68763118739428:8739439:8747619:8747756:8832063:88321968747619:8747756ENSG00000166444.13ENST00000528527.1
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENSG00000166444.13ENST00000534127.1,ENST00000313726.6,ENST00000357665.1
exon_skip_68771118747619:8747756:8772167:8772272:8832063:88321968772167:8772272ENSG00000166444.13ENST00000530438.1,ENST00000533425.1,ENST00000527510.1
exon_skip_68773118747619:8747756:8772167:8772272:8832793:88328828772167:8772272ENSG00000166444.13ENST00000533225.1,ENST00000526126.1
exon_skip_68779118772167:8772272:8832793:8832882:8853102:88532358832793:8832882ENSG00000166444.13ENST00000533225.1,ENST00000526126.1,ENST00000530959.1,ENST00000527392.1,ENST00000526828.1,ENST00000525169.1
exon_skip_68780118772167:8772272:8832793:8832882:8860856:88608978832793:8832882ENSG00000166444.13ENST00000534127.1,ENST00000357665.1,ENST00000527347.1,ENST00000527516.1,ENST00000524757.1,ENST00000534665.1
exon_skip_68782118772167:8772272:8832793:8832882:8892500:88925318832793:8832882ENSG00000166444.13ENST00000526155.1,ENST00000533471.1
exon_skip_68784118772167:8772272:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000530938.1
exon_skip_68791118772167:8772272:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000526241.1
exon_skip_68794118832829:8832878:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000531640.1
exon_skip_68799118832793:8832882:8853102:8853235:8860856:88608978853102:8853235ENSG00000166444.13ENST00000532651.1,ENST00000526126.1,ENST00000525169.1
exon_skip_68801118832793:8832882:8853102:8853235:8892500:88925318853102:8853235ENSG00000166444.13ENST00000527392.1
exon_skip_68807118832793:8832882:8860856:8860897:8892381:88924648860856:8860897ENSG00000166444.13ENST00000527347.1
exon_skip_68808118832793:8832882:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000527516.1,ENST00000534665.1
exon_skip_68810118832793:8832882:8860856:8860897:8902556:89026568860856:8860897ENSG00000166444.13ENST00000534127.1
exon_skip_68814118832793:8832882:8892500:8892635:8892880:88929148892500:8892635ENSG00000166444.13ENST00000533471.1
exon_skip_68819118853102:8853235:8860856:8860897:8892500:88925318860856:8860897ENSG00000166444.13ENST00000526126.1,ENST00000530938.1,ENST00000525169.1
exon_skip_68823118860856:8860897:8878889:8878983:8892500:88926358878889:8878983ENSG00000166444.13ENST00000524757.1
exon_skip_68824118860856:8860897:8892500:8892635:8892880:88929148892500:8892635ENSG00000166444.13ENST00000527516.1,ENST00000525169.1
exon_skip_68827118860856:8860897:8902556:8902656:8932367:89324988902556:8902656ENSG00000166444.13ENST00000534127.1

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 ST5

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
ENST00000534127883279388328823UTR-3UTR
ENST00000534127886085688608973UTR-3UTR
ENST0000031372687207598720937Frame-shift
ENST0000053412787207598720937Frame-shift
ENST0000031372687241188724267Frame-shift
ENST0000053412787241188724267Frame-shift
ENST0000031372687326688732778Frame-shift
ENST0000053412787326688732778Frame-shift
ENST0000031372687340978734282Frame-shift
ENST0000053412787340978734282Frame-shift
ENST0000031372687476198747756Frame-shift
ENST0000053412787476198747756Frame-shift
ENST0000031372687179738718213In-frame
ENST0000053412787179738718213In-frame
ENST0000031372687204798720521In-frame
ENST0000053412787204798720521In-frame
ENST0000031372687293238729401In-frame
ENST0000053412787293238729401In-frame
ENST0000031372687355448735589In-frame
ENST0000053412787355448735589In-frame
ENST0000031372687371498737365In-frame
ENST0000053412787371498737365In-frame
ENST0000031372687514968752756In-frame
ENST0000053412787514968752756In-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
ENST00000534127883279388328823UTR-3UTR
ENST00000534127886085688608973UTR-3UTR
ENST00000534127890255689026563UTR-3UTR
ENST0000031372687207598720937Frame-shift
ENST0000053412787207598720937Frame-shift
ENST0000031372687241188724267Frame-shift
ENST0000053412787241188724267Frame-shift
ENST0000031372687326688732778Frame-shift
ENST0000053412787326688732778Frame-shift
ENST0000031372687340978734282Frame-shift
ENST0000053412787340978734282Frame-shift
ENST0000031372687476198747756Frame-shift
ENST0000053412787476198747756Frame-shift
ENST0000031372687179738718213In-frame
ENST0000053412787179738718213In-frame
ENST0000031372687204798720521In-frame
ENST0000053412787204798720521In-frame
ENST0000031372687293238729401In-frame
ENST0000053412787293238729401In-frame
ENST0000031372687355448735589In-frame
ENST0000053412787355448735589In-frame
ENST0000031372687371498737365In-frame
ENST0000053412787371498737365In-frame
ENST0000031372687514968752756In-frame
ENST0000053412787514968752756In-frame

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Infer the effects of exon skipping event on protein functional features for ST5

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
ENST000003137264524113787514968752756430168927446
ENST000005341274562113787514968752756467172627446
ENST00000313726452411378737149873736519792194543615
ENST00000534127456211378737149873736520162231543615
ENST00000313726452411378735544873558922922336647662
ENST00000534127456211378735544873558923292373647662
ENST00000313726452411378729323872940127022779784810
ENST00000534127456211378729323872940127392816784810
ENST00000313726452411378720479872052132483289966980
ENST00000534127456211378720479872052132853326966980
ENST0000031372645241137871797387182133402364110171097
ENST0000053412745621137871797387182133439367810171097

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
ENST000003137264524113787514968752756430168927446
ENST000005341274562113787514968752756467172627446
ENST00000313726452411378737149873736519792194543615
ENST00000534127456211378737149873736520162231543615
ENST00000313726452411378735544873558922922336647662
ENST00000534127456211378735544873558923292373647662
ENST00000313726452411378729323872940127022779784810
ENST00000534127456211378729323872940127392816784810
ENST00000313726452411378720479872052132483289966980
ENST00000534127456211378720479872052132853326966980
ENST0000031372645241137871797387182133402364110171097
ENST0000053412745621137871797387182133439367810171097

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 ST5

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.
ST5_COAD_exon_skip_68768_psi_boxplot.png
boxplot
ST5_ESCA_exon_skip_68768_psi_boxplot.png
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ST5_GBM_exon_skip_68768_psi_boxplot.png
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ST5_HNSC_exon_skip_68768_psi_boxplot.png
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ST5_LIHC_exon_skip_68768_psi_boxplot.png
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ST5_LUSC_exon_skip_68768_psi_boxplot.png
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ST5_STAD_exon_skip_68768_psi_boxplot.png
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check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-DD-A1EG-01exon_skip_68682
exon_skip_68683
8720760872093787208208720820Frame_Shift_DelG-p.P946fs
UCECTCGA-D1-A0ZO-01exon_skip_68746
8732669873277887326778732678Frame_Shift_DelCT-p.E758fs
LIHCTCGA-DD-A1EG-01exon_skip_68750
8734098873428287341708734170Frame_Shift_DelA-p.F700fs
LIHCTCGA-DD-A1EG-01exon_skip_68750
8734098873428287341798734179Frame_Shift_DelA-p.F697fs
LIHCTCGA-DD-A1EG-01exon_skip_68754
8737150873736587371678737167Frame_Shift_DelC-p.A610fs
COADTCGA-AD-5900-01exon_skip_68768
8751497875275687515548751554Frame_Shift_DelG-p.P428fs
LIHCTCGA-G3-A3CJ-01exon_skip_68768
8751497875275687515648751564Frame_Shift_DelT-p.T425fs
STADTCGA-BR-8487-01exon_skip_68768
8751497875275687517988751798Frame_Shift_DelC-p.E347fs
LIHCTCGA-DD-A39Y-01exon_skip_68768
8751497875275687521248752124Frame_Shift_DelG-p.P238fs
GBMTCGA-06-0882-01exon_skip_68768
8751497875275687521668752166Frame_Shift_DelC-p.G224fs
LIHCTCGA-CC-A5UE-01exon_skip_68768
8751497875275687524478752447Frame_Shift_DelG-p.A130fs
LIHCTCGA-CC-A5UE-01exon_skip_68768
8751497875275687524478752447Frame_Shift_DelG-p.C131fs
LIHCTCGA-DD-A1EG-01exon_skip_68768
8751497875275687525648752564Frame_Shift_DelG-p.T91fs
LIHCTCGA-DD-A3A0-01exon_skip_68768
8751497875275687525678752567Frame_Shift_DelG-p.P90fs
STADTCGA-BR-4362-01exon_skip_68768
8751497875275687526198752619Frame_Shift_DelG-p.P73fs
UCECTCGA-AP-A05N-01exon_skip_68768
8751497875275687526198752619Frame_Shift_DelG-p.P73fs
HNSCTCGA-CV-7099-01exon_skip_68713
8724119872426787241648724164Nonsense_MutationGCp.S892*
STADTCGA-CD-5801-01exon_skip_68746
8732669873277887326938732693Nonsense_MutationCTp.W753*
STADTCGA-CD-5801-01exon_skip_68746
8732669873277887326938732693Nonsense_MutationCTp.W753X
UCECTCGA-D1-A16E-01exon_skip_68750
8734098873428287341398734139Nonsense_MutationGAp.R711*
HNSCTCGA-CV-A6K2-01exon_skip_68754
8737150873736587372298737229Nonsense_MutationGCp.S589*
UCECTCGA-BS-A0UV-01exon_skip_68763
exon_skip_68762
exon_skip_68761
8747620874775687476448747644Nonsense_MutationCAp.E485*
ESCATCGA-IC-A6RE-01exon_skip_68768
8751497875275687517108751710Nonsense_MutationGTp.S376*
ESCATCGA-IC-A6RE-01exon_skip_68768
8751497875275687517108751710Nonsense_MutationGTp.S376X
HNSCTCGA-CV-A6JD-01exon_skip_68768
8751497875275687517108751710Nonsense_MutationGTp.S376*
LUSCTCGA-63-5131-01exon_skip_68768
8751497875275687517418751741Nonsense_MutationCAp.G366*
STADTCGA-HU-A4GN-01exon_skip_68768
8751497875275687523248752324Nonsense_MutationCTp.W171*
STADTCGA-HU-A4GN-01exon_skip_68768
8751497875275687523248752324Nonsense_MutationCTp.W171X
COADTCGA-G4-6588-01exon_skip_68768
8751497875275687526058752605Nonsense_MutationGAp.Q78X

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-G4-6588-01Sample: TCGA-G4-6588-01
Cancer type: COAD
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8752605
Mutation end: 8752605
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: A
AAchange: p.Q78X
exon_skip_135806_COAD_TCGA-G4-6588-01.png
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exon_skip_136696_COAD_TCGA-G4-6588-01.png
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exon_skip_313058_COAD_TCGA-G4-6588-01.png
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exon_skip_322889_COAD_TCGA-G4-6588-01.png
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exon_skip_322890_COAD_TCGA-G4-6588-01.png
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exon_skip_330818_COAD_TCGA-G4-6588-01.png
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exon_skip_382354_COAD_TCGA-G4-6588-01.png
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exon_skip_386802_COAD_TCGA-G4-6588-01.png
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exon_skip_4028_COAD_TCGA-G4-6588-01.png
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exon_skip_434039_COAD_TCGA-G4-6588-01.png
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exon_skip_434040_COAD_TCGA-G4-6588-01.png
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exon_skip_5121_COAD_TCGA-G4-6588-01.png
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exon_skip_5861_COAD_TCGA-G4-6588-01.png
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exon_skip_68768_COAD_TCGA-G4-6588-01.png
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exon_skip_76742_COAD_TCGA-G4-6588-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-IC-A6RE-01Sample: TCGA-IC-A6RE-01
Cancer type: ESCA
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751710
Mutation end: 8751710
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: T
AAchange: p.S376X
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-IC-A6RE-01Sample: TCGA-IC-A6RE-01
Cancer type: ESCA
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751710
Mutation end: 8751710
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: T
AAchange: p.S376*
exon_skip_379913_ESCA_TCGA-IC-A6RE-01.png
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exon_skip_499409_ESCA_TCGA-IC-A6RE-01.png
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exon_skip_68768_ESCA_TCGA-IC-A6RE-01.png
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exon_skip_80515_ESCA_TCGA-IC-A6RE-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-CV-A6JD-01Sample: TCGA-CV-A6JD-01
Cancer type: HNSC
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751710
Mutation end: 8751710
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: T
AAchange: p.S376*
exon_skip_68768_HNSC_TCGA-CV-A6JD-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-63-5131-01Sample: TCGA-63-5131-01
Cancer type: LUSC
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751741
Mutation end: 8751741
Mutation type: Nonsense_Mutation
Reference seq: C
Mutation seq: A
AAchange: p.G366*
exon_skip_68768_LUSC_TCGA-63-5131-01.png
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exon_skip_97740_LUSC_TCGA-63-5131-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-AD-5900-01Sample: TCGA-AD-5900-01
Cancer type: COAD
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751554
Mutation end: 8751554
Mutation type: Frame_Shift_Del
Reference seq: G
Mutation seq: -
AAchange: p.P428fs
exon_skip_123601_COAD_TCGA-AD-5900-01.png
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exon_skip_135806_COAD_TCGA-AD-5900-01.png
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exon_skip_146733_COAD_TCGA-AD-5900-01.png
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exon_skip_291928_COAD_TCGA-AD-5900-01.png
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exon_skip_303809_COAD_TCGA-AD-5900-01.png
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exon_skip_315782_COAD_TCGA-AD-5900-01.png
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exon_skip_367235_COAD_TCGA-AD-5900-01.png
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exon_skip_376149_COAD_TCGA-AD-5900-01.png
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exon_skip_457524_COAD_TCGA-AD-5900-01.png
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exon_skip_459148_COAD_TCGA-AD-5900-01.png
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exon_skip_68768_COAD_TCGA-AD-5900-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-06-0882-01Sample: TCGA-06-0882-01
Cancer type: GBM
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8752166
Mutation end: 8752166
Mutation type: Frame_Shift_Del
Reference seq: C
Mutation seq: -
AAchange: p.G224fs
exon_skip_68768_GBM_TCGA-06-0882-01.png
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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_68683
Skipped exon start: 8720760
Skipped exon end: 8720937
Mutation start: 8720820
Mutation end: 8720820
Mutation type: Frame_Shift_Del
Reference seq: G
Mutation seq: -
AAchange: p.P946fs
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_68750
Skipped exon start: 8734098
Skipped exon end: 8734282
Mutation start: 8734170
Mutation end: 8734170
Mutation type: Frame_Shift_Del
Reference seq: A
Mutation seq: -
AAchange: p.F700fs
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_68750
Skipped exon start: 8734098
Skipped exon end: 8734282
Mutation start: 8734179
Mutation end: 8734179
Mutation type: Frame_Shift_Del
Reference seq: A
Mutation seq: -
AAchange: p.F697fs
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_68754
Skipped exon start: 8737150
Skipped exon end: 8737365
Mutation start: 8737167
Mutation end: 8737167
Mutation type: Frame_Shift_Del
Reference seq: C
Mutation seq: -
AAchange: p.A610fs
ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-DD-A1EG-01Sample: TCGA-DD-A1EG-01
Cancer type: LIHC
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8752564
Mutation end: 8752564
Mutation type: Frame_Shift_Del
Reference seq: G
Mutation seq: -
AAchange: p.T91fs
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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ST5_8747619_8747756_8751496_8752756_8772167_8772272_TCGA-BR-8487-01Sample: TCGA-BR-8487-01
Cancer type: STAD
ESID: exon_skip_68768
Skipped exon start: 8751497
Skipped exon end: 8752756
Mutation start: 8751798
Mutation end: 8751798
Mutation type: Frame_Shift_Del
Reference seq: C
Mutation seq: -
AAchange: p.E347fs
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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
SISO_CERVIX8751497875275687517918751791Frame_Shift_DelC-p.G349fs
GRST_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687517918751791Frame_Shift_DelC-p.G349fs
LNCAPCLONEFGC_PROSTATE8751497875275687526198752619Frame_Shift_DelG-p.P73fs
U266B1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687516188751619Frame_Shift_Ins-Gp.S407fs
EN_ENDOMETRIUM8751497875275687518508751851Frame_Shift_Ins-Cp.G329fs
SNU1040_LARGE_INTESTINE8717974871821387180038718003Missense_MutationTCp.D1088G
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8717974871821387180588718058Missense_MutationGAp.R1070C
IHH4_THYROID8717974871821387180908718090Missense_MutationGAp.A1059V
JHUEM7_ENDOMETRIUM8717974871821387181458718145Missense_MutationAGp.Y1041H
SNUC5_LARGE_INTESTINE8717974871821387181748718174Missense_MutationATp.I1031N
HT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8720760872093787208398720839Missense_MutationAGp.I940T
BCPAP_THYROID8720760872093787208438720843Missense_MutationCTp.D939N
HEC251_ENDOMETRIUM8724119872426787241768724176Missense_MutationCTp.R888Q
HEC108_ENDOMETRIUM8724119872426787241888724188Missense_MutationCTp.R884H
PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8724119872426787241898724189Missense_MutationGAp.R884C
SKMEL2_SKIN8724119872426787242078724207Missense_MutationAGp.F878L
TOV21G_OVARY8724119872426787242258724225Missense_MutationCTp.V872M
NALM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8724119872426787242258724225Missense_MutationCTp.V872M
GP2D_LARGE_INTESTINE8732669873277887326788732678Missense_MutationTCp.E758G
GP5D_LARGE_INTESTINE8732669873277887326788732678Missense_MutationTCp.E758G
YD10B_UPPER_AERODIGESTIVE_TRACT8734098873428287341418734141Missense_MutationGAp.S710L
CHLA06ATRT_SOFT_TISSUE8735545873558987355708735570Missense_MutationCGp.E654D
ES1_BONE8737150873736587371558737155Missense_MutationGAp.P614S
PACADD137_PANCREAS8737150873736587371608737160Missense_MutationCTp.R612H
HT29_LARGE_INTESTINE8737150873736587371748737174Missense_MutationGCp.S607R
RCCFG2_KIDNEY8737150873736587372668737266Missense_MutationCTp.D577N
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8737150873736587372748737274Missense_MutationCAp.S574I
LS513_LARGE_INTESTINE8737150873736587372968737296Missense_MutationGCp.P567A
HCT15_LARGE_INTESTINE8737150873736587373358737335Missense_MutationGAp.R554C
MLMA_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8747620874775687476348747634Missense_MutationTCp.Y488C
HCC202_BREAST8747620874775687476838747683Missense_MutationCTp.E472K
SNU1040_LARGE_INTESTINE8751497875275687515128751512Missense_MutationCTp.R442H
JHC7_BONE8751497875275687515218751521Missense_MutationCGp.R439P
CMLT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687515228751522Missense_MutationGAp.R439C
HEC6_ENDOMETRIUM8751497875275687515428751542Missense_MutationCTp.R432Q
HEC251_ENDOMETRIUM8751497875275687515578751557Missense_MutationGAp.A427V
KYSE450_OESOPHAGUS8751497875275687515768751576Missense_MutationGCp.P421A
NCIH64_LUNG8751497875275687515798751579Missense_MutationGAp.P420S
JHESOAD1_OESOPHAGUS8751497875275687516238751623Missense_MutationTCp.K405R
NALM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687516488751648Missense_MutationCTp.E397K
BONNA12_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687517948751794Missense_MutationGAp.A348V
SNU175_LARGE_INTESTINE8751497875275687519448751944Missense_MutationCTp.R298Q
HCT15_LARGE_INTESTINE8751497875275687519458751945Missense_MutationGAp.R298W
HEC59_ENDOMETRIUM8751497875275687520238752023Missense_MutationGAp.H272Y
U698M_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687520488752048Missense_MutationACp.S263R
HUNS1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687520528752052Missense_MutationCTp.R262Q
BICR56_UPPER_AERODIGESTIVE_TRACT8751497875275687520748752074Missense_MutationGAp.R255W
NUGC3_STOMACH8751497875275687521618752161Missense_MutationGAp.R226W
TC138_BONE8751497875275687521888752188Missense_MutationCGp.E217Q
RKO_LARGE_INTESTINE8751497875275687522578752257Missense_MutationCTp.E194K
CW2_LARGE_INTESTINE8751497875275687522988752298Missense_MutationCAp.R180M
SNU1040_LARGE_INTESTINE8751497875275687523438752343Missense_MutationCTp.R165Q
HCT116_LARGE_INTESTINE8751497875275687523658752365Missense_MutationGAp.R158C
TGBC11TKB_STOMACH8751497875275687524768752476Missense_MutationCTp.A121T
TC71_BONE8751497875275687524938752493Missense_MutationTCp.K115R
HEC108_ENDOMETRIUM8751497875275687525248752524Missense_MutationTCp.S105G
CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE8751497875275687525478752547Missense_MutationGAp.A97V
NCIH441_LUNG8751497875275687526868752686Missense_MutationCTp.E51K
TOV21G_OVARY8751497875275687527428752742Missense_MutationGTp.S32Y
BICR18_UPPER_AERODIGESTIVE_TRACT8772168877227287721808772180Missense_MutationCTp.G23E
OV7_OVARY8772168877227287721868772186Missense_MutationGAp.P21L
MZ7MEL_SKIN8772168877227287722198772219Missense_MutationCTp.S10N
HEC59_ENDOMETRIUM8737150873736587372938737293Nonsense_MutationGAp.R568*
UMUC3_URINARY_TRACT8737150873736587373198737319Nonsense_MutationGCp.S559*
D458_CENTRAL_NERVOUS_SYSTEM8732669873277887327768732777Splice_SiteCAATp.L725H
HCC2108_LUNG8734098873428287340998734099Splice_SiteTCp.K724R

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ST5

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value
exon_skip_68784118772167:8772272:8853102:8853235:8860856:88608978853102:8853235ENST00000530938.1PRADrs2251536chr11:8853177G/C2.06e-03
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1GBMrs3812762chr11:8751640C/G8.91e-04
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1ESCArs3812762chr11:8751640C/G6.09e-07
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1BRCArs3812762chr11:8751640C/G4.91e-13
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1LGGrs3812762chr11:8751640C/G3.01e-13
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1KIRCrs3812762chr11:8751640C/G1.14e-06
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1LUADrs3812762chr11:8751640C/G2.98e-04
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1LUSCrs3794153chr11:8751889C/G1.44e-10
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1LUSCrs3812762chr11:8751640C/G3.58e-07
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1OVrs3812762chr11:8751640C/G6.24e-08
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1PAADrs3812762chr11:8751640C/G8.80e-05
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1PRADrs3812762chr11:8751640C/G2.94e-05
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1PRADrs3794153chr11:8751889C/G5.22e-05
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1PRADrs3794153chr11:8751889C/G3.20e-04
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1PRADrs3812762chr11:8751640C/G2.51e-03
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1SARCrs3812762chr11:8751640C/G5.55e-04
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1STADrs3794153chr11:8751889C/G3.12e-09
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1STADrs3812762chr11:8751640C/G3.19e-08
exon_skip_68768118747619:8747756:8751496:8752756:8772167:87722728751496:8752756ENST00000534127.1,ENST00000313726.6,ENST00000357665.1THCArs3812762chr11:8751640C/G6.52e-11
exon_skip_68794118832829:8832878:8853102:8853235:8860856:88608978853102:8853235ENST00000531640.1PRADrs2251536chr11:8853177G/C2.06e-03
exon_skip_68801118832793:8832882:8853102:8853235:8892500:88925318853102:8853235ENST00000527392.1PRADrs2251536chr11:8853177G/C2.06e-03
exon_skip_68799118832793:8832882:8853102:8853235:8860856:88608978853102:8853235ENST00000525169.1,ENST00000526126.1,ENST00000532651.1PRADrs2251536chr11:8853177G/C2.06e-03

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ST5


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ST5


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RelatedDrugs for ST5

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 ST5

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