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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 BIRC6

check button Gene summary
Gene informationGene symbol

BIRC6

Gene ID

57448

Gene namebaculoviral IAP repeat containing 6
SynonymsAPOLLON|BRUCE
Cytomap

2p22.3

Type of geneprotein-coding
Descriptionbaculoviral IAP repeat-containing protein 6BIR repeat-containing ubiquitin-conjugating enzymeRING-type E3 ubiquitin transferase BIRC6ubiquitin-conjugating BIR-domain enzyme apollon
Modification date20180523
UniProtAcc

Q9NR09

ContextPubMed: BIRC6 [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 BIRC6 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 BIRC6

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 BIRC6

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_324663232602655:32602837:32605220:32605358:32613817:3261401132605220:32605358ENSG00000115760.9ENST00000421745.2
exon_skip_324665232613878:32614011:32617106:32617218:32620578:3262066132617106:32617218ENSG00000115760.9ENST00000421745.2,ENST00000466527.1
exon_skip_324667232626230:32626453:32626530:32626691:32631566:3263162532626530:32626691ENSG00000115760.9ENST00000421745.2
exon_skip_324668232626530:32626691:32631566:32631625:32639836:3264123132631566:32631625ENSG00000115760.9ENST00000421745.2
exon_skip_324670232658717:32658872:32660563:32660653:32661120:3266125232660563:32660653ENSG00000115760.9ENST00000421745.2
exon_skip_324671232658715:32658872:32661120:32661252:32664575:3266475432661120:32661252ENSG00000115760.9ENST00000444173.1
exon_skip_324672232664575:32664754:32666396:32666530:32667132:3266729432666396:32666530ENSG00000115760.9ENST00000421745.2
exon_skip_324675232670588:32670736:32673862:32673996:32678875:3267901032673862:32673996ENSG00000115760.9ENST00000421745.2
exon_skip_324679232673862:32673996:32678875:32679010:32688261:3268844932678875:32679010ENSG00000115760.9ENST00000421745.2
exon_skip_324682232688261:32688449:32689576:32689891:32690132:3269023232689576:32689891ENSG00000115760.9ENST00000421745.2
exon_skip_324683232689576:32689891:32690132:32690232:32692592:3269280732690132:32690232ENSG00000115760.9ENST00000421745.2
exon_skip_324684232690132:32690232:32692592:32692807:32692970:3269317932692592:32692807ENSG00000115760.9ENST00000421745.2
exon_skip_324685232692970:32693179:32693504:32693851:32694462:3269468232693504:32693851ENSG00000115760.9ENST00000421745.2
exon_skip_324687232701280:32701412:32702435:32702651:32703702:3270388632702435:32702651ENSG00000115760.9ENST00000421745.2
exon_skip_324688232704529:32704685:32706387:32706521:32707496:3270765032706387:32706521ENSG00000115760.9ENST00000421745.2
exon_skip_324689232710709:32710826:32712713:32712868:32713654:3271378132712713:32712868ENSG00000115760.9ENST00000421745.2
exon_skip_324690232713654:32713781:32715107:32715218:32716491:3271662532715107:32715218ENSG00000115760.9ENST00000421745.2
exon_skip_324691232718606:32718734:32724613:32725176:32726779:3272695532724613:32725176ENSG00000115760.9ENST00000421745.2
exon_skip_324692232733046:32733326:32734804:32735061:32735592:3273570132734804:32735061ENSG00000115760.9ENST00000421745.2
exon_skip_324696232737999:32738221:32740056:32740837:32743320:3274346432740056:32740837ENSG00000115760.9ENST00000421745.2
exon_skip_324700232743883:32744013:32749954:32750086:32750530:3275069532749954:32750086ENSG00000115760.9ENST00000421745.2
exon_skip_324702232756421:32756618:32768307:32768608:32770709:3277092732768307:32768608ENSG00000115760.9ENST00000471232.1,ENST00000421745.2
exon_skip_324703232772916:32773081:32774379:32774548:32800222:3280043332774379:32774548ENSG00000115760.9ENST00000471232.1,ENST00000421745.2
exon_skip_324704232774379:32774548:32800222:32800433:32815872:3281604532800222:32800433ENSG00000115760.9ENST00000471232.1
exon_skip_324705232774379:32774548:32800222:32800433:32818981:3281912732800222:32800433ENSG00000115760.9ENST00000421745.2
exon_skip_324711232800357:32800433:32815872:32816045:32818981:3281912732815872:32816045ENSG00000115760.9ENST00000471232.1
exon_skip_324714232800357:32800433:32818981:32819127:32820100:3282021132818981:32819127ENSG00000115760.9ENST00000421745.2
exon_skip_324719232818981:32819127:32820100:32820211:32822817:3282303532820100:32820211ENSG00000115760.9ENST00000471232.1,ENST00000421745.2
exon_skip_324727232828072:32828150:32832521:32832710:32836514:3283664832832521:32832710ENSG00000115760.9ENST00000465130.1,ENST00000471232.1,ENST00000421745.2
exon_skip_324728232832521:32832710:32836514:32836649:32842791:3284394332836514:32836649ENSG00000115760.9ENST00000471232.1,ENST00000421745.2

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

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Exon skipping events with PSIs in GTEx for BIRC6

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_324663232602655:32602837:32605220:32605358:32613817:3261401132605220:32605358ENSG00000115760.9ENST00000421745.2
exon_skip_324665232613878:32614011:32617106:32617218:32620578:3262066132617106:32617218ENSG00000115760.9ENST00000421745.2,ENST00000466527.1
exon_skip_324667232626230:32626453:32626530:32626691:32631566:3263162532626530:32626691ENSG00000115760.9ENST00000421745.2
exon_skip_324668232626530:32626691:32631566:32631625:32639836:3264123132631566:32631625ENSG00000115760.9ENST00000421745.2
exon_skip_324670232658717:32658872:32660563:32660653:32661120:3266125232660563:32660653ENSG00000115760.9ENST00000421745.2
exon_skip_324671232658715:32658872:32661120:32661252:32664575:3266475432661120:32661252ENSG00000115760.9ENST00000444173.1
exon_skip_324672232664575:32664754:32666396:32666530:32667132:3266729432666396:32666530ENSG00000115760.9ENST00000421745.2
exon_skip_324675232670588:32670736:32673862:32673996:32678875:3267901032673862:32673996ENSG00000115760.9ENST00000421745.2
exon_skip_324679232673862:32673996:32678875:32679010:32688261:3268844932678875:32679010ENSG00000115760.9ENST00000421745.2
exon_skip_324682232688261:32688449:32689576:32689891:32690132:3269023232689576:32689891ENSG00000115760.9ENST00000421745.2
exon_skip_324683232689576:32689891:32690132:32690232:32692592:3269280732690132:32690232ENSG00000115760.9ENST00000421745.2
exon_skip_324684232690132:32690232:32692592:32692807:32692970:3269317932692592:32692807ENSG00000115760.9ENST00000421745.2
exon_skip_324685232692970:32693179:32693504:32693851:32694462:3269468232693504:32693851ENSG00000115760.9ENST00000421745.2
exon_skip_324687232701280:32701412:32702435:32702651:32703702:3270388632702435:32702651ENSG00000115760.9ENST00000421745.2
exon_skip_324688232704529:32704685:32706387:32706521:32707496:3270765032706387:32706521ENSG00000115760.9ENST00000421745.2
exon_skip_324689232710709:32710826:32712713:32712868:32713654:3271378132712713:32712868ENSG00000115760.9ENST00000421745.2
exon_skip_324690232713654:32713781:32715107:32715218:32716491:3271662532715107:32715218ENSG00000115760.9ENST00000421745.2
exon_skip_324691232718606:32718734:32724613:32725176:32726779:3272695532724613:32725176ENSG00000115760.9ENST00000421745.2
exon_skip_324692232733046:32733326:32734804:32735061:32735592:3273570132734804:32735061ENSG00000115760.9ENST00000421745.2
exon_skip_324696232737999:32738221:32740056:32740837:32743320:3274346432740056:32740837ENSG00000115760.9ENST00000421745.2
exon_skip_324700232743883:32744013:32749954:32750086:32750530:3275069532749954:32750086ENSG00000115760.9ENST00000421745.2
exon_skip_324702232756421:32756618:32768307:32768608:32770709:3277092732768307:32768608ENSG00000115760.9ENST00000421745.2,ENST00000471232.1
exon_skip_324704232774379:32774548:32800222:32800433:32815872:3281604532800222:32800433ENSG00000115760.9ENST00000471232.1
exon_skip_324705232774379:32774548:32800222:32800433:32818981:3281912732800222:32800433ENSG00000115760.9ENST00000421745.2
exon_skip_324711232800357:32800433:32815872:32816045:32818981:3281912732815872:32816045ENSG00000115760.9ENST00000471232.1
exon_skip_324714232800357:32800433:32818981:32819127:32820100:3282021132818981:32819127ENSG00000115760.9ENST00000421745.2
exon_skip_324719232818981:32819127:32820100:32820211:32822817:3282303532820100:32820211ENSG00000115760.9ENST00000421745.2,ENST00000471232.1
exon_skip_324727232828072:32828150:32832521:32832710:32836514:3283664832832521:32832710ENSG00000115760.9ENST00000421745.2,ENST00000471232.1,ENST00000465130.1
exon_skip_324728232832521:32832710:32836514:32836649:32842791:3284394332836514:32836649ENSG00000115760.9ENST00000421745.2,ENST00000471232.1

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 BIRC6

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
ENST000004217453261710632617218Frame-shift
ENST000004217453262653032626691Frame-shift
ENST000004217453263156632631625Frame-shift
ENST000004217453266639632666530Frame-shift
ENST000004217453267386232673996Frame-shift
ENST000004217453269013232690232Frame-shift
ENST000004217453269259232692807Frame-shift
ENST000004217453269350432693851Frame-shift
ENST000004217453270638732706521Frame-shift
ENST000004217453271271332712868Frame-shift
ENST000004217453272461332725176Frame-shift
ENST000004217453273480432735061Frame-shift
ENST000004217453274005632740837Frame-shift
ENST000004217453276830732768608Frame-shift
ENST000004217453277437932774548Frame-shift
ENST000004217453280022232800433Frame-shift
ENST000004217453281898132819127Frame-shift
ENST000004217453260522032605358In-frame
ENST000004217453266056332660653In-frame
ENST000004217453267887532679010In-frame
ENST000004217453268957632689891In-frame
ENST000004217453270243532702651In-frame
ENST000004217453271510732715218In-frame
ENST000004217453274995432750086In-frame
ENST000004217453282010032820211In-frame
ENST000004217453283252132832710In-frame
ENST000004217453283651432836649In-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
ENST000004217453261710632617218Frame-shift
ENST000004217453262653032626691Frame-shift
ENST000004217453263156632631625Frame-shift
ENST000004217453266639632666530Frame-shift
ENST000004217453267386232673996Frame-shift
ENST000004217453269013232690232Frame-shift
ENST000004217453269259232692807Frame-shift
ENST000004217453269350432693851Frame-shift
ENST000004217453270638732706521Frame-shift
ENST000004217453271271332712868Frame-shift
ENST000004217453272461332725176Frame-shift
ENST000004217453273480432735061Frame-shift
ENST000004217453274005632740837Frame-shift
ENST000004217453276830732768608Frame-shift
ENST000004217453280022232800433Frame-shift
ENST000004217453281898132819127Frame-shift
ENST000004217453260522032605358In-frame
ENST000004217453266056332660653In-frame
ENST000004217453267887532679010In-frame
ENST000004217453268957632689891In-frame
ENST000004217453270243532702651In-frame
ENST000004217453271510732715218In-frame
ENST000004217453274995432750086In-frame
ENST000004217453282010032820211In-frame
ENST000004217453283252132832710In-frame
ENST000004217453283651432836649In-frame

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Infer the effects of exon skipping event on protein functional features for BIRC6

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
ENST000004217451572048573260522032605358642779169215
ENST0000042174515720485732660563326606533544363311361166
ENST0000042174515720485732678875326790104753488715391584
ENST0000042174515720485732689576326898915076539016471752
ENST0000042174515720485732702435327026516987720222842356
ENST0000042174515720485732715107327152188230834026982735
ENST000004217451572048573274995432750086117581188938743918
ENST000004217451572048573282010032820211136361374645004537
ENST000004217451572048573283252132832710142051439346904753
ENST000004217451572048573283651432836649143941452847534798

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
ENST000004217451572048573260522032605358642779169215
ENST0000042174515720485732660563326606533544363311361166
ENST0000042174515720485732678875326790104753488715391584
ENST0000042174515720485732689576326898915076539016471752
ENST0000042174515720485732702435327026516987720222842356
ENST0000042174515720485732715107327152188230834026982735
ENST000004217451572048573274995432750086117581188938743918
ENST000004217451572048573282010032820211136361374645004537
ENST000004217451572048573283252132832710142051439346904753
ENST000004217451572048573283651432836649143941452847534798

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
Q9NR0916921514857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091136116614857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091539158414857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091647175214857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091647175216601668Compositional biasNote=Poly-Ala
Q9NR091647175217101710Modified residueNote=Phosphothreonine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:24275569;Dbxref=PMID:24275569
Q9NR092284235614857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR092284235623192319Sequence conflictNote=L->F;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q9NR092698273514857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR093874391814857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094500453745364540Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094500453714857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094500453745244533HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475314857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094690475346884698HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347044707HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347114714HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347184738HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347414745HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347524777HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475345764704RegionNote=Ubiquitin-conjugating
Q9NR094690475347494751TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094753479814857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094753479847524777HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094753479847884810HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG


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
Q9NR0916921514857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091136116614857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091539158414857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091647175214857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR091647175216601668Compositional biasNote=Poly-Ala
Q9NR091647175217101710Modified residueNote=Phosphothreonine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:24275569;Dbxref=PMID:24275569
Q9NR092284235614857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR092284235623192319Sequence conflictNote=L->F;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q9NR092698273514857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR093874391814857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094500453745364540Beta strandOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094500453714857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094500453745244533HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475314857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094690475346884698HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347044707HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347114714HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347184738HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347414745HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475347524777HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094690475345764704RegionNote=Ubiquitin-conjugating
Q9NR094690475347494751TurnOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094753479814857ChainID=PRO_0000122361;Note=Baculoviral IAP repeat-containing protein 6
Q9NR094753479847524777HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG
Q9NR094753479847884810HelixOntology_term=ECO:0000244;evidence=ECO:0000244|PDB:3CEG


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SNVs in the skipped exons for BIRC6

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.
BIRC6_COAD_exon_skip_324696_psi_boxplot.png
boxplot
BIRC6_LIHC_exon_skip_324696_psi_boxplot.png
boxplot
BIRC6_PAAD_exon_skip_324675_psi_boxplot.png
boxplot
BIRC6_STAD_exon_skip_324696_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
LIHCTCGA-DD-A3A0-01exon_skip_324667
32626531326266913262668632626686Frame_Shift_DelA-p.G471fs
KIRPTCGA-AL-3472-01exon_skip_324670
32660564326606533266061832660618Frame_Shift_DelA-p.E1155fs
KIRPTCGA-AL-3472-01exon_skip_324670
32660564326606533266061832660618Frame_Shift_DelA-p.E1156fs
LIHCTCGA-G3-A3CJ-01exon_skip_324672
32666397326665303266644932666449Frame_Shift_DelA-p.E1288fs
LIHCTCGA-G3-A3CJ-01exon_skip_324682
32689577326898913268972932689729Frame_Shift_DelA-p.P1698fs
COADTCGA-D5-6927-01exon_skip_324682
32689577326898913268983832689838Frame_Shift_DelC-p.D1734fs
LIHCTCGA-G3-A3CJ-01exon_skip_324683
32690133326902323269018032690180Frame_Shift_DelT-p.H1768fs
LIHCTCGA-DD-A39Y-01exon_skip_324684
32692593326928073269261832692618Frame_Shift_DelT-p.D1794fs
LIHCTCGA-G3-A3CJ-01exon_skip_324684
32692593326928073269267832692678Frame_Shift_DelT-p.S1814fs
LIHCTCGA-DD-A1EG-01exon_skip_324687
32702436327026513270251332702513Frame_Shift_DelA-p.A2310fs
LGGTCGA-HT-7608-01exon_skip_324688
32706388327065213270640732706407Frame_Shift_DelT-p.S2476fs
LIHCTCGA-DD-A3A0-01exon_skip_324689
32712714327128683271275232712752Frame_Shift_DelG-p.G2619fs
LIHCTCGA-DD-A1EG-01exon_skip_324689
32712714327128683271283732712837Frame_Shift_DelT-p.L2646fs
LIHCTCGA-DD-A3A0-01exon_skip_324691
32724614327251763272482532724825Frame_Shift_DelG-p.G2895fs
LIHCTCGA-DD-A1EG-01exon_skip_324696
32740057327408373274015632740156Frame_Shift_DelT-p.Y3556fs
COADTCGA-G4-6588-01exon_skip_324696
32740057327408373274023832740238Frame_Shift_DelA-p.S3583fs
BLCATCGA-4Z-AA84-01exon_skip_324696
32740057327408373274056432740577Frame_Shift_DelAGTTGGCAATAGCC-p.VGNSH3693fs
STADTCGA-CG-4476-01exon_skip_324696
32740057327408373274073732740740Frame_Shift_DelGACT-p.3750_3751del
STADTCGA-CG-4476-01exon_skip_324696
32740057327408373274073732740740Frame_Shift_DelGACT-p.G3750fs
LIHCTCGA-G3-A3CJ-01exon_skip_324700
32749955327500863275001132750011Frame_Shift_DelA-p.K3894fs
LIHCTCGA-DD-A1EG-01exon_skip_324700
32749955327500863275004532750045Frame_Shift_DelA-p.E3905fs
LIHCTCGA-G3-A3CJ-01exon_skip_324700
32749955327500863275004532750045Frame_Shift_DelA-p.E3905fs
LIHCTCGA-DD-A1EG-01exon_skip_324702
32768308327686083276839232768392Frame_Shift_DelG-p.G4126fs
LIHCTCGA-DD-A3A1-01exon_skip_324728
32836515328366493283660932836609Frame_Shift_DelG-p.R4785fs
COADTCGA-AA-3492-01exon_skip_324663
32605221326053583260531232605313Frame_Shift_Ins-Ap.L200fs
STADTCGA-CG-4449-01exon_skip_324675
32673863326739963267387532673876Frame_Shift_Ins-Ap.Y1499fs
STADTCGA-CG-4449-01exon_skip_324675
32673863326739963267387632673877Frame_Shift_Ins-Ap.Y1499fs
LIHCTCGA-BC-A10S-01exon_skip_324682
32689577326898913268968132689682Frame_Shift_Ins-Gp.AP1682fs
UCECTCGA-AX-A0IS-01exon_skip_324685
32693505326938513269352832693529Frame_Shift_Ins-Gp.L1935fs
UCECTCGA-D1-A0ZP-01exon_skip_324685
32693505326938513269352832693529Frame_Shift_Ins-Gp.L1935fs
LIHCTCGA-BC-A112-01exon_skip_324685
32693505326938513269362932693630Frame_Shift_Ins-Gp.G1969fs
KIRPTCGA-WN-AB4C-01exon_skip_324696
32740057327408373274015932740160Frame_Shift_Ins-TCp.F3557fs
STADTCGA-BR-4184-01exon_skip_324728
32836515328366493283652832836529Frame_Shift_Ins-Tp.H4758fs
STADTCGA-BR-4184-01exon_skip_324728
32836515328366493283652932836530Frame_Shift_Ins-Tp.H4758fs
KIRPTCGA-HE-7130-01exon_skip_324667
32626531326266913262657932626579Nonsense_MutationCTp.Q436*
KIRPTCGA-HE-7130-01exon_skip_324667
32626531326266913262657932626579Nonsense_MutationCTp.Q436X
LUSCTCGA-18-3406-01exon_skip_324689
32712714327128683271273132712731Nonsense_MutationGTp.G2611*
STADTCGA-CG-5718-01exon_skip_324690
32715108327152183271511132715111Nonsense_MutationCGp.S2700*
STADTCGA-CG-5718-01exon_skip_324690
32715108327152183271511132715111Nonsense_MutationCGp.S2700X
UCECTCGA-D1-A103-01exon_skip_324691
32724614327251763272466632724666Nonsense_MutationGTp.E2841*
HNSCTCGA-CV-7095-01exon_skip_324691
32724614327251763272476632724766Nonsense_MutationCGp.S2874*
DLBCTCGA-FA-8693-01exon_skip_324691
32724614327251763272481332724813Nonsense_MutationCTp.R2890X
STADTCGA-BR-8680-01exon_skip_324700
32749955327500863275002932750029Nonsense_MutationGTp.E3900*
UCECTCGA-A5-A0GP-01exon_skip_324700
32749955327500863275002932750029Nonsense_MutationGTp.E3900*
SKCMTCGA-D9-A6EC-06exon_skip_324702
32768308327686083276857232768572Nonsense_MutationCTp.R4186*
SKCMTCGA-D9-A6EC-06exon_skip_324702
32768308327686083276857232768572Nonsense_MutationCTp.R4186X
THYMTCGA-XU-A931-01exon_skip_324703
32774380327745483277448832774488Nonsense_MutationGTp.E4362X
BLCATCGA-BT-A3PJ-01exon_skip_324727
32832522328327103283264532832645Nonsense_MutationCTp.R4732*
UCECTCGA-BS-A0UF-01exon_skip_324727
32832522328327103283264532832645Nonsense_MutationCTp.R4732*
ACCTCGA-OR-A5KB-01exon_skip_324675
32673863326739963267386232673862Splice_SiteGT.
LUADTCGA-95-7043-01exon_skip_324675
32673863326739963267386232673862Splice_SiteGTp.R1495_splice
PAADTCGA-IB-7651-01exon_skip_324675
32673863326739963267399732673997Splice_SiteGA.
LIHCTCGA-DD-AACE-01exon_skip_324703
32774380327745483277437832774378Splice_SiteAG.
READTCGA-EI-6882-01exon_skip_324719
32820101328202113282010032820101Splice_Site-A.
UCECTCGA-D1-A0ZO-01exon_skip_324719
32820101328202113282010032820101Splice_Site-Ap.E4501_splice
BRCATCGA-A8-A081-01exon_skip_324728
32836515328366493283651432836514Splice_SiteGTe73-1

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
BIRC6_32737999_32738221_32740056_32740837_32743320_32743464_TCGA-CG-4476-01Sample: TCGA-CG-4476-01
Cancer type: STAD
ESID: exon_skip_324696
Skipped exon start: 32740057
Skipped exon end: 32740837
Mutation start: 32740737
Mutation end: 32740740
Mutation type: Frame_Shift_Del
Reference seq: GACT
Mutation seq: -
AAchange: p.3750_3751del
BIRC6_32737999_32738221_32740056_32740837_32743320_32743464_TCGA-CG-4476-01Sample: TCGA-CG-4476-01
Cancer type: STAD
ESID: exon_skip_324696
Skipped exon start: 32740057
Skipped exon end: 32740837
Mutation start: 32740737
Mutation end: 32740740
Mutation type: Frame_Shift_Del
Reference seq: GACT
Mutation seq: -
AAchange: p.G3750fs
exon_skip_30081_STAD_TCGA-CG-4476-01.png
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exon_skip_324696_STAD_TCGA-CG-4476-01.png
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exon_skip_325485_STAD_TCGA-CG-4476-01.png
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BIRC6_32670588_32670736_32673862_32673996_32678875_32679010_TCGA-IB-7651-01Sample: TCGA-IB-7651-01
Cancer type: PAAD
ESID: exon_skip_324675
Skipped exon start: 32673863
Skipped exon end: 32673996
Mutation start: 32673997
Mutation end: 32673997
Mutation type: Splice_Site
Reference seq: G
Mutation seq: A
AAchange: .
exon_skip_113241_PAAD_TCGA-IB-7651-01.png
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exon_skip_115380_PAAD_TCGA-IB-7651-01.png
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exon_skip_124564_PAAD_TCGA-IB-7651-01.png
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exon_skip_135806_PAAD_TCGA-IB-7651-01.png
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exon_skip_139341_PAAD_TCGA-IB-7651-01.png
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exon_skip_153733_PAAD_TCGA-IB-7651-01.png
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exon_skip_155805_PAAD_TCGA-IB-7651-01.png
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exon_skip_18053_PAAD_TCGA-IB-7651-01.png
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exon_skip_18056_PAAD_TCGA-IB-7651-01.png
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exon_skip_23067_PAAD_TCGA-IB-7651-01.png
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exon_skip_287059_PAAD_TCGA-IB-7651-01.png
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exon_skip_294631_PAAD_TCGA-IB-7651-01.png
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exon_skip_298512_PAAD_TCGA-IB-7651-01.png
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exon_skip_306900_PAAD_TCGA-IB-7651-01.png
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exon_skip_307723_PAAD_TCGA-IB-7651-01.png
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exon_skip_315960_PAAD_TCGA-IB-7651-01.png
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exon_skip_324675_PAAD_TCGA-IB-7651-01.png
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exon_skip_330351_PAAD_TCGA-IB-7651-01.png
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exon_skip_334330_PAAD_TCGA-IB-7651-01.png
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exon_skip_341784_PAAD_TCGA-IB-7651-01.png
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exon_skip_343314_PAAD_TCGA-IB-7651-01.png
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exon_skip_348329_PAAD_TCGA-IB-7651-01.png
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exon_skip_354232_PAAD_TCGA-IB-7651-01.png
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exon_skip_370626_PAAD_TCGA-IB-7651-01.png
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exon_skip_377740_PAAD_TCGA-IB-7651-01.png
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exon_skip_385032_PAAD_TCGA-IB-7651-01.png
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exon_skip_390031_PAAD_TCGA-IB-7651-01.png
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exon_skip_422548_PAAD_TCGA-IB-7651-01.png
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exon_skip_424536_PAAD_TCGA-IB-7651-01.png
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exon_skip_431753_PAAD_TCGA-IB-7651-01.png
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exon_skip_432982_PAAD_TCGA-IB-7651-01.png
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exon_skip_435489_PAAD_TCGA-IB-7651-01.png
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exon_skip_435729_PAAD_TCGA-IB-7651-01.png
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exon_skip_441705_PAAD_TCGA-IB-7651-01.png
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exon_skip_448879_PAAD_TCGA-IB-7651-01.png
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exon_skip_468347_PAAD_TCGA-IB-7651-01.png
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exon_skip_494000_PAAD_TCGA-IB-7651-01.png
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exon_skip_494029_PAAD_TCGA-IB-7651-01.png
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exon_skip_499410_PAAD_TCGA-IB-7651-01.png
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exon_skip_499695_PAAD_TCGA-IB-7651-01.png
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exon_skip_499697_PAAD_TCGA-IB-7651-01.png
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exon_skip_79905_PAAD_TCGA-IB-7651-01.png
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exon_skip_80096_PAAD_TCGA-IB-7651-01.png
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exon_skip_95924_PAAD_TCGA-IB-7651-01.png
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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
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32689577326898913268983832689838Frame_Shift_DelC-p.P1736fs
HPBALL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32706388327065213270651432706514Frame_Shift_DelT-p.V2512fs
BICR18_UPPER_AERODIGESTIVE_TRACT32724614327251763272506132725064Frame_Shift_DelTGTT-p.SV2972fs
NCIH2009_LUNG32740057327408373274053632740548Frame_Shift_DelTTGCTCCTATTCT-p.VAPIL3683fs
BICR18_UPPER_AERODIGESTIVE_TRACT32724614327251763272506632725067Frame_Shift_Ins-CTCCp.QG2974fs
EN_ENDOMETRIUM32749955327500863274999032749991Frame_Shift_Ins-Ap.Q3887fs
JHH2_LIVER32689577326898913268961132689619In_Frame_DelCAGCTGCAG-p.AAA1663del
SNUC4_LARGE_INTESTINE32800223328004333280034532800347In_Frame_DelGAA-p.E4425del
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32605221326053583260524532605245Missense_MutationTAp.L178I
BICR18_UPPER_AERODIGESTIVE_TRACT32605221326053583260524532605245Missense_MutationTAp.L178I
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32605221326053583260525432605254Missense_MutationGAp.V181I
BICR18_UPPER_AERODIGESTIVE_TRACT32605221326053583260525432605254Missense_MutationGAp.V181I
SCC4_UPPER_AERODIGESTIVE_TRACT32605221326053583260525532605255Missense_MutationTCp.V181A
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32605221326053583260526032605260Missense_MutationAGp.I183V
BICR18_UPPER_AERODIGESTIVE_TRACT32605221326053583260526032605260Missense_MutationAGp.I183V
CW2_LARGE_INTESTINE32605221326053583260530532605305Missense_MutationGAp.D198N
SKGIIIA_CERVIX32617107326172183261715132617151Missense_MutationCTp.S295L
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32660564326606533266058632660586Missense_MutationATp.Q1144H
BICR18_UPPER_AERODIGESTIVE_TRACT32660564326606533266058632660586Missense_MutationATp.Q1144H
S117_SOFT_TISSUE32660564326606533266058632660586Missense_MutationATp.Q1144H
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32660564326606533266059532660595Missense_MutationACp.K1147N
BICR18_UPPER_AERODIGESTIVE_TRACT32660564326606533266059532660595Missense_MutationACp.K1147N
S117_SOFT_TISSUE32660564326606533266059532660595Missense_MutationACp.K1147N
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32660564326606533266062832660628Missense_MutationGCp.Q1158H
BICR18_UPPER_AERODIGESTIVE_TRACT32660564326606533266062832660628Missense_MutationGCp.Q1158H
EPLC272H_LUNG32661121326612523266117732661177Missense_MutationGAp.V1186I
DV90_LUNG32661121326612523266121432661214Missense_MutationCTp.A1198V
NCIH2286_LUNG32661121326612523266121732661217Missense_MutationGTp.G1199V
SW756_CERVIX32661121326612523266123232661232Missense_MutationCGp.T1204R
SW156_KIDNEY32666397326665303266643032666430Missense_MutationATp.S1282C
CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32666397326665303266645832666458Missense_MutationGAp.R1291Q
UMCHOR1_BONE32673863326739963267386532673865Missense_MutationAGp.Y1496C
HT115_LARGE_INTESTINE32673863326739963267398832673988Missense_MutationTCp.V1537A
BEN_LUNG32678876326790103267888132678881Missense_MutationGAp.G1542R
MKN1_STOMACH32678876326790103267889132678891Missense_MutationGCp.S1545T
NCIH596_LUNG32678876326790103267892432678924Missense_MutationCTp.S1556F
MOLT16_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32678876326790103267893832678938Missense_MutationTGp.L1561V
HCC33_LUNG32678876326790103267895832678958Missense_MutationCGp.H1567Q
SNU245_BILIARY_TRACT32689577326898913268962832689628Missense_MutationGAp.A1665T
MEWO_SKIN32689577326898913268964332689643Missense_MutationGAp.G1670S
HCC70_BREAST32689577326898913268965032689650Missense_MutationTCp.V1672A
LS411N_LARGE_INTESTINE32689577326898913268966132689661Missense_MutationGAp.V1676M
SNU466_CENTRAL_NERVOUS_SYSTEM32689577326898913268969732689697Missense_MutationAGp.I1688V
KMS28BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32689577326898913268971532689715Missense_MutationAGp.I1694V
NCIH2291_LUNG32689577326898913268980932689809Missense_MutationCTp.A1725V
NCIH596_LUNG32689577326898913268985632689856Missense_MutationGCp.A1741P
NCIH838_LUNG32689577326898913268986032689860Missense_MutationCTp.A1742V
HT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32689577326898913268987732689877Missense_MutationACp.N1748H
JHUEM1_ENDOMETRIUM32690133326902323269022332690223Missense_MutationAGp.M1783V
MG63_BONE32690133326902323269022532690225Missense_MutationGAp.M1783I
HCC2450_LUNG32692593326928073269275432692754Missense_MutationCGp.H1840D
NCIH2172_LUNG32692593326928073269275432692754Missense_MutationCGp.H1840D
NCIH630_LARGE_INTESTINE32693505326938513269352532693525Missense_MutationGAp.R1934H
HCE4_OESOPHAGUS32693505326938513269356032693560Missense_MutationCTp.P1946S
LN443_CENTRAL_NERVOUS_SYSTEM32693505326938513269366232693662Missense_MutationCGp.L1980V
LK2_LUNG32693505326938513269377332693773Missense_MutationAGp.T2017A
IGROV1_OVARY32702436327026513270246632702466Missense_MutationAGp.T2295A
NCIH1793_LUNG32702436327026513270247532702475Missense_MutationTAp.W2298R
HUNS1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32702436327026513270258632702586Missense_MutationCTp.L2335F
SKMEL5_SKIN32702436327026513270262832702628Missense_MutationGAp.D2349N
SMSCTR_SOFT_TISSUE32706388327065213270649832706498Missense_MutationCTp.P2507S
SNU719_STOMACH32712714327128683271283732712837Missense_MutationTGp.L2646R
JHH5_LIVER32712714327128683271285532712855Missense_MutationTGp.V2652G
MKN7_STOMACH32724614327251763272464332724643Missense_MutationTAp.L2833H
JHUEM7_ENDOMETRIUM32724614327251763272482232724822Missense_MutationTGp.F2893V
BT20_BREAST32724614327251763272484932724849Missense_MutationCTp.R2902C
PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32724614327251763272487732724877Missense_MutationGAp.G2911D
KPL1_BREAST32724614327251763272488932724889Missense_MutationGAp.R2915K
NCIH1793_LUNG32724614327251763272491132724911Missense_MutationGTp.L2922F
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32724614327251763272495132724951Missense_MutationGAp.G2936S
BICR18_UPPER_AERODIGESTIVE_TRACT32724614327251763272495132724951Missense_MutationGAp.G2936S
SNU1040_LARGE_INTESTINE32724614327251763272500632725006Missense_MutationTCp.V2954A
CW2_LARGE_INTESTINE32724614327251763272504232725042Missense_MutationGTp.G2966V
DAUDI_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32724614327251763272504232725042Missense_MutationGTp.G2966V
DMS153_LUNG32724614327251763272510532725105Missense_MutationAGp.N2987S
CP66MEL_SKIN32724614327251763272516932725169Missense_MutationGAp.M3008I
JHU022_UPPER_AERODIGESTIVE_TRACT32734805327350613273483632734836Missense_MutationCGp.L3338V
UW228_CENTRAL_NERVOUS_SYSTEM32734805327350613273487432734874Missense_MutationTAp.S3350R
ES6_BONE32734805327350613273504732735047Missense_MutationGAp.G3408D
SKMEL2_SKIN32740057327408373274012732740127Missense_MutationTCp.C3547R
LS411N_LARGE_INTESTINE32740057327408373274014532740145Missense_MutationCAp.H3553N
HCC2998_LARGE_INTESTINE32740057327408373274020932740209Missense_MutationAGp.H3574R
SNU626_CENTRAL_NERVOUS_SYSTEM32740057327408373274022332740223Missense_MutationAGp.M3579V
HEC108_ENDOMETRIUM32740057327408373274030432740304Missense_MutationAGp.T3606A
MZ1B_MATCHED_NORMAL_TISSUE32740057327408373274048432740484Missense_MutationCTp.R3666C
MZ1PC_PANCREAS32740057327408373274048432740484Missense_MutationCTp.R3666C
HT115_LARGE_INTESTINE32740057327408373274049432740494Missense_MutationTCp.V3669A
NCIH1048_LUNG32740057327408373274051732740517Missense_MutationCTp.P3677S
LS411N_LARGE_INTESTINE32740057327408373274051832740518Missense_MutationCAp.P3677H
LOVO_LARGE_INTESTINE32740057327408373274052932740529Missense_MutationGAp.D3681N
CMK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32740057327408373274065932740659Missense_MutationCGp.S3724C
CMK115_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32740057327408373274065932740659Missense_MutationCGp.S3724C
BE2M17_AUTONOMIC_GANGLIA32740057327408373274075432740754Missense_MutationCTp.R3756C
SKNBE2_AUTONOMIC_GANGLIA32740057327408373274075432740754Missense_MutationCTp.R3756C
GMEL_SKIN32749955327500863274998132749981Missense_MutationAGp.I3884V
FUOV1_OVARY32768308327686083276832332768323Missense_MutationGTp.V4103L
HEC108_ENDOMETRIUM32768308327686083276832932768329Missense_MutationTCp.S4105P
HS274T_BREAST32768308327686083276838432768384Missense_MutationAGp.E4123G
HPAFII_PANCREAS32768308327686083276838432768384Missense_MutationAGp.E4123G
SF172_CENTRAL_NERVOUS_SYSTEM32768308327686083276846232768462Missense_MutationCAp.T4149N
VMRCLCD_LUNG32768308327686083276854932768549Missense_MutationGTp.R4178I
JHUEM7_ENDOMETRIUM32768308327686083276857332768573Missense_MutationGAp.R4186Q
GA10_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32768308327686083276857732768577Missense_MutationGTp.L4187F
NCIH1651_LUNG32768308327686083276859632768596Missense_MutationGAp.D4194N
H3118_UPPER_AERODIGESTIVE_TRACT32774380327745483277438332774383Missense_MutationCTp.L4327F
HEC1_ENDOMETRIUM32774380327745483277440432774404Missense_MutationGAp.V4334I
NCIH1651_LUNG32774380327745483277441432774414Missense_MutationCTp.A4337V
MM386_SKIN32774380327745483277453732774537Missense_MutationGCp.R4378P
MM386_SKIN32774380327745483277454232774542Missense_MutationGAp.D4380N
HEC108_ENDOMETRIUM32800223328004333280023232800232Missense_MutationTCp.M4385T
KM12_LARGE_INTESTINE32800223328004333280027732800277Missense_MutationGCp.R4400P
MHHCALL4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32800223328004333280029732800297Missense_MutationGTp.A4407S
SNU1040_LARGE_INTESTINE32800223328004333280029832800298Missense_MutationCTp.A4407V
OCILY3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32800223328004333280040132800401Missense_MutationGCp.K4441N
PL4_PANCREAS32818982328191273281899832818998Missense_MutationGAp.V4458I
NCIH748_LUNG32818982328191273281900432819004Missense_MutationAGp.T4460A
IM95_STOMACH32818982328191273281906432819064Missense_MutationGAp.D4480N
HCC2218_BREAST32820101328202113282010832820108Missense_MutationACp.K4503N
SNU1040_LARGE_INTESTINE32820101328202113282013132820131Missense_MutationCTp.A4511V
LNZTA3WT4_CENTRAL_NERVOUS_SYSTEM32820101328202113282015732820157Missense_MutationGCp.V4520L
LNZ308_CENTRAL_NERVOUS_SYSTEM32820101328202113282015732820157Missense_MutationGCp.V4520L
RL952_ENDOMETRIUM32832522328327103283257732832577Missense_MutationCTp.P4709L
NCIH1694_LUNG32832522328327103283267832832678Missense_MutationCGp.Q4743E
CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE32836515328366493283654032836540Missense_MutationACp.K4762T
KYSE520_OESOPHAGUS32836515328366493283662732836627Missense_MutationCAp.S4791Y
CAR1_LARGE_INTESTINE32836515328366493283664232836642Missense_MutationCGp.A4796G
HCET_UPPER_AERODIGESTIVE_TRACT32690133326902323269022032690220Nonsense_MutationCTp.R1782*
647V_URINARY_TRACT32693505326938513269375032693750Nonsense_MutationCGp.S2009*
CW2_LARGE_INTESTINE32774380327745483277453632774536Nonsense_MutationCTp.R4378*
NCIH1155_LUNG32774380327745483277453632774536Nonsense_MutationCTp.R4378*
KMH2_THYROID32820101328202113282016732820167Nonsense_MutationCAp.S4523*
MM426_SKIN32832522328327103283262432832624Nonsense_MutationCTp.R4725*
HCC1569_BREAST32631567326316253263162432631624Splice_SiteAGp.T492T
NCIH2172_LUNG32740057327408373274083732740837Splice_SiteG-p.Q3783fs
BICR18_UPPER_AERODIGESTIVE_TRACT32768308327686083276860732768607Splice_SiteACp.G4197G
SNU520_STOMACH32820101328202113282010132820101Splice_SiteA-p.E4501fs
LS411N_LARGE_INTESTINE32820101328202113282010132820101Splice_SiteA-p.E4501fs
MCC13_SKIN32836515328366493283664932836650Splice_SiteGGAAp.K4798K
MCC13_SKIN32836515328366493283664932836649Splice_SiteGAp.K4798K

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for BIRC6

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 BIRC6


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for BIRC6


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RelatedDrugs for BIRC6

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 BIRC6

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