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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 ANKRD11

check button Gene summary
Gene informationGene symbol

ANKRD11

Gene ID

29123

Gene nameankyrin repeat domain 11
SynonymsANCO-1|ANCO1|LZ16|T13
Cytomap

16q24.3

Type of geneprotein-coding
Descriptionankyrin repeat domain-containing protein 11ankyrin repeat-containing cofactor 1nasopharyngeal carcinoma susceptibility proteintruncated ankyrin repeat domain 11 aberrant transcript 1truncated ankyrin repeat domain 11 aberrant transcript 2
Modification date20180523
UniProtAcc

Q6UB99

ContextPubMed: ANKRD11 [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 ANKRD11 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 ANKRD11

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 ANKRD11

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1470191689334940:89335071:89337224:89337317:89341221:8934136589337224:89337317ENSG00000167522.10ENST00000330736.5,ENST00000378330.2,ENST00000562194.1,ENST00000301030.4
exon_skip_1470221689341221:89341365:89341500:89341599:89345479:8935205789341500:89341599ENSG00000167522.10ENST00000330736.5,ENST00000378330.2,ENST00000301030.4
exon_skip_1470241689341500:89341599:89345479:89352057:89352446:8935259489345479:89352057ENSG00000167522.10ENST00000330736.5,ENST00000378330.2,ENST00000301030.4
exon_skip_1470361689357420:89357591:89358088:89358185:89371613:8937175289358088:89358185ENSG00000167522.10ENST00000330736.5,ENST00000378332.2,ENST00000562275.1
exon_skip_1470401689357420:89357591:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000378330.2,ENST00000301030.4
exon_skip_1470441689358135:89358185:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000330736.5,ENST00000562816.1,ENST00000562275.1
exon_skip_1473231689367173:89367370:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000563291.1,ENST00000566858.1,ENST00000567736.1
exon_skip_1473291689371613:89371752:89379724:89379997:89383340:8938348389379724:89379997ENSG00000167522.10ENST00000378332.2
exon_skip_1473301689371613:89371752:89383340:89383483:89484691:8948476589383340:89383483ENSG00000167522.10ENST00000562816.1
exon_skip_1473321689371613:89371752:89383340:89383486:89484691:8948476589383340:89383486ENSG00000167522.10ENST00000378330.2,ENST00000301030.4
exon_skip_1473571689383340:89383486:89484691:89484776:89556652:8955670189484691:89484776ENSG00000167522.10ENST00000301030.4,ENST00000378332.2

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

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Exon skipping events with PSIs in GTEx for ANKRD11

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1470191689334940:89335071:89337224:89337317:89341221:8934136589337224:89337317ENSG00000167522.10ENST00000378330.2,ENST00000301030.4,ENST00000330736.5,ENST00000562194.1
exon_skip_1470221689341221:89341365:89341500:89341599:89345479:8935205789341500:89341599ENSG00000167522.10ENST00000378330.2,ENST00000301030.4,ENST00000330736.5
exon_skip_1470241689341500:89341599:89345479:89352057:89352446:8935259489345479:89352057ENSG00000167522.10ENST00000378330.2,ENST00000301030.4,ENST00000330736.5
exon_skip_1470361689357420:89357591:89358088:89358185:89371613:8937175289358088:89358185ENSG00000167522.10ENST00000330736.5,ENST00000562275.1,ENST00000378332.2
exon_skip_1470401689357420:89357591:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000378330.2,ENST00000301030.4
exon_skip_1470441689358135:89358185:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000330736.5,ENST00000562275.1,ENST00000562816.1
exon_skip_1473231689367173:89367370:89371613:89371752:89383340:8938348389371613:89371752ENSG00000167522.10ENST00000567736.1,ENST00000563291.1,ENST00000566858.1
exon_skip_1473291689371613:89371752:89379724:89379997:89383340:8938348389379724:89379997ENSG00000167522.10ENST00000378332.2
exon_skip_1473301689371613:89371752:89383340:89383483:89484691:8948476589383340:89383483ENSG00000167522.10ENST00000562816.1
exon_skip_1473321689371613:89371752:89383340:89383486:89484691:8948476589383340:89383486ENSG00000167522.10ENST00000378330.2,ENST00000301030.4
exon_skip_1473571689383340:89383486:89484691:89484776:89556652:8955670189484691:89484776ENSG00000167522.10ENST00000301030.4,ENST00000378332.2

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 ANKRD11

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
ENST0000030103089383340893834863UTR-3CDS
ENST0000037833089383340893834863UTR-3CDS
ENST0000030103089484691894847763UTR-3UTR
ENST000003010308934547989352057Frame-shift
ENST000003783308934547989352057Frame-shift
ENST000003010308937161389371752Frame-shift
ENST000003783308937161389371752Frame-shift
ENST000003010308933722489337317In-frame
ENST000003783308933722489337317In-frame
ENST000003010308934150089341599In-frame
ENST000003783308934150089341599In-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
ENST0000030103089383340893834863UTR-3CDS
ENST0000037833089383340893834863UTR-3CDS
ENST0000030103089484691894847763UTR-3UTR
ENST000003010308934547989352057Frame-shift
ENST000003783308934547989352057Frame-shift
ENST000003010308937161389371752Frame-shift
ENST000003783308937161389371752Frame-shift
ENST000003010308933722489337317In-frame
ENST000003783308933722489337317In-frame
ENST000003010308934150089341599In-frame
ENST000003783308934150089341599In-frame

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Infer the effects of exon skipping event on protein functional features for ANKRD11

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
ENST000003010309318266389341500893415997932803024902523
ENST000003783309146266389341500893415997760785824902523
ENST000003010309318266389337224893373178175826725712602
ENST000003783309146266389337224893373178003809525712602

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
ENST000003010309318266389341500893415997932803024902523
ENST000003783309146266389341500893415997760785824902523
ENST000003010309318266389337224893373178175826725712602
ENST000003783309146266389337224893373178003809525712602

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
Q6UB992490252312663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992490252312663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992490252325122512Natural variantID=VAR_075870;Note=In KBGS%3B unknown pathological significance. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252325122512Natural variantID=VAR_075870;Note=In KBGS%3B unknown pathological significance. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252323692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252323692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992571260212663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992571260212663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992571260223692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992571260223692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698


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
Q6UB992490252312663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992490252312663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992490252325122512Natural variantID=VAR_075870;Note=In KBGS%3B unknown pathological significance. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252325122512Natural variantID=VAR_075870;Note=In KBGS%3B unknown pathological significance. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252323692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992490252323692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992571260212663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992571260212663ChainID=PRO_0000066907;Note=Ankyrin repeat domain-containing protein 11
Q6UB992571260223692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698
Q6UB992571260223692663RegionNote=Important for protein degradation;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:25413698;Dbxref=PMID:25413698


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SNVs in the skipped exons for ANKRD11

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.
ANKRD11_BRCA_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_COAD_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_ESCA_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_HNSC_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_SKCM_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_STAD_exon_skip_147024_psi_boxplot.png
boxplot
ANKRD11_UCEC_exon_skip_147024_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-A1EG-01exon_skip_147024
89345480893520578934643789346437Frame_Shift_DelG-p.P2171fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578934696289346962Frame_Shift_DelG-p.P1996fs
LIHCTCGA-DD-A3A0-01exon_skip_147024
89345480893520578934701889347018Frame_Shift_DelC-p.D1978fs
STADTCGA-HU-A4G8-01exon_skip_147024
89345480893520578934732089347320Frame_Shift_DelG-p.P1877fs
LIHCTCGA-DD-A39Y-01exon_skip_147024
89345480893520578934762989347629Frame_Shift_DelT-p.N1774fs
LIHCTCGA-G3-A3CJ-01exon_skip_147024
89345480893520578934762989347629Frame_Shift_DelT-p.N1774fs
SKCMTCGA-EE-A20C-06exon_skip_147024
89345480893520578934783289347832Frame_Shift_DelA-p.P1706fs
SKCMTCGA-EE-A20C-06exon_skip_147024
89345480893520578934783289347832Frame_Shift_DelA-p.T1707fs
SKCMTCGA-EE-A185-06exon_skip_147024
89345480893520578934790889347908Frame_Shift_DelG-p.A1681fs
LIHCTCGA-DD-A39Y-01exon_skip_147024
89345480893520578934809689348096Frame_Shift_DelG-p.P1618fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578934815089348150Frame_Shift_DelC-p.R1600fs
LIHCTCGA-DD-A3A0-01exon_skip_147024
89345480893520578934850189348501Frame_Shift_DelC-p.G1483fs
LIHCTCGA-DD-A39Y-01exon_skip_147024
89345480893520578934851889348518Frame_Shift_DelC-p.D1478fs
BLCATCGA-DK-A3WW-01exon_skip_147024
89345480893520578934857389348573Frame_Shift_DelC-p.K1459fs
BLCATCGA-DK-A3WW-01exon_skip_147024
89345480893520578934857389348573Frame_Shift_DelC-p.K1461fs
KIRCTCGA-CZ-5462-01exon_skip_147024
89345480893520578934904389349043Frame_Shift_DelC-p.V1303fs
COADTCGA-G4-6628-01exon_skip_147024
89345480893520578934935689349356Frame_Shift_DelT-p.E1199fs
STADTCGA-BR-8361-01exon_skip_147024
89345480893520578934935689349356Frame_Shift_DelT-p.E1199fs
STADTCGA-BR-8361-01exon_skip_147024
89345480893520578934935689349356Frame_Shift_DelT-p.K1198fs
BLCATCGA-GV-A3JZ-01exon_skip_147024
89345480893520578934965189349651Frame_Shift_DelG-p.S1100fs
STADTCGA-HU-A4GN-01exon_skip_147024
89345480893520578934983889349838Frame_Shift_DelT-p.S1038fs
LIHCTCGA-DD-A3A0-01exon_skip_147024
89345480893520578934987889349878Frame_Shift_DelT-p.K1024fs
LIHCTCGA-G3-A3CJ-01exon_skip_147024
89345480893520578934987889349878Frame_Shift_DelT-p.K1024fs
SKCMTCGA-EE-A183-06exon_skip_147024
89345480893520578934989189349895Frame_Shift_DelTTCCT-p.1019_1020del
SKCMTCGA-EE-A183-06exon_skip_147024
89345480893520578934989189349895Frame_Shift_DelTTCCT-p.RK1019fs
LIHCTCGA-G3-A3CJ-01exon_skip_147024
89345480893520578935045089350450Frame_Shift_DelA-p.S834fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578935048889350488Frame_Shift_DelT-p.N821fs
LIHCTCGA-G3-A3CJ-01exon_skip_147024
89345480893520578935053889350538Frame_Shift_DelT-p.K804fs
UCECTCGA-B5-A0K9-01exon_skip_147024
89345480893520578935053889350538Frame_Shift_DelT-p.K804fs
KIRCTCGA-BP-5198-01exon_skip_147024
89345480893520578935069289350692Frame_Shift_DelG-p.P753fs
LIHCTCGA-DD-A3A0-01exon_skip_147024
89345480893520578935086289350862Frame_Shift_DelT-p.K696fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578935098489350984Frame_Shift_DelT-p.S656fs
LIHCTCGA-DD-A3A0-01exon_skip_147024
89345480893520578935100289351002Frame_Shift_DelG-p.Q650fs
COADTCGA-AZ-4615-01exon_skip_147024
89345480893520578935159589351595Frame_Shift_DelT-p.N452fs
ESCATCGA-JY-A6FG-01exon_skip_147024
89345480893520578935163789351637Frame_Shift_DelT-p.K438fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578935175489351754Frame_Shift_DelG-p.P399fs
LIHCTCGA-DD-A39Y-01exon_skip_147024
89345480893520578935176989351769Frame_Shift_DelT-p.N395fs
LIHCTCGA-DD-A39Y-01exon_skip_147024
89345480893520578935179489351794Frame_Shift_DelT-p.M386fs
LIHCTCGA-DD-A1EG-01exon_skip_147024
89345480893520578935181089351810Frame_Shift_DelA-p.F380fs
KIRPTCGA-G7-A8LB-01exon_skip_147323
exon_skip_147040
exon_skip_147044
89371614893717528937169689371696Frame_Shift_DelC-p.K49fs
PRADTCGA-J9-A52C-01exon_skip_147024
89345480893520578934935589349356Frame_Shift_Ins-Tp.E1199fs
ESCATCGA-L5-A4OI-01exon_skip_147024
89345480893520578934964089349641Frame_Shift_Ins-Tp.*1104fs
ESCATCGA-L5-A4OI-01exon_skip_147024
89345480893520578934964089349641Frame_Shift_Ins-Tp.D1103fs
ESCATCGA-L5-A88S-01exon_skip_147024
89345480893520578934964089349641Frame_Shift_Ins-Tp.D1103fs
STADTCGA-BR-7851-01exon_skip_147024
89345480893520578934964089349641Frame_Shift_Ins-Tp.D1104fs
STADTCGA-BR-7851-01exon_skip_147024
89345480893520578934964189349642Frame_Shift_Ins-Tp.K1103fs
STADTCGA-SW-A7EA-01exon_skip_147024
89345480893520578935105689351057Frame_Shift_Ins-Tp.*632fs
STADTCGA-SW-A7EA-01exon_skip_147024
89345480893520578935105689351057Frame_Shift_Ins-Tp.H632fs
DLBCTCGA-GS-A9TU-01exon_skip_147024
89345480893520578935172189351722Frame_Shift_Ins-Tp.T410fs
BRCATCGA-BH-A0DK-01exon_skip_147024
89345480893520578935174689351747Frame_Shift_Ins-Tp.A401fs
BLCATCGA-DK-AA71-01exon_skip_147024
89345480893520578934632289346322Nonsense_MutationCAp.E2210*
BLCATCGA-FD-A62P-01exon_skip_147024
89345480893520578934729989347299Nonsense_MutationGCp.S1884*
BRCATCGA-B6-A0IB-01exon_skip_147024
89345480893520578934763389347633Nonsense_MutationCAp.E1773*
BLCATCGA-CF-A47X-01exon_skip_147024
89345480893520578934835689348356Nonsense_MutationCAp.E1532*
LGGTCGA-E1-A7YN-01exon_skip_147024
89345480893520578934885789348857Nonsense_MutationGAp.R1365*
BLCATCGA-FD-A6TG-01exon_skip_147024
89345480893520578934890889348908Nonsense_MutationCAp.E1348*
BLCATCGA-DK-AA71-01exon_skip_147024
89345480893520578934901989349019Nonsense_MutationGAp.R1311*
COADTCGA-F4-6570-01exon_skip_147024
89345480893520578934901989349019Nonsense_MutationGAp.R1311X
SKCMTCGA-FR-A3YO-06exon_skip_147024
89345480893520578934948189349481Nonsense_MutationCAp.E1157*
SKCMTCGA-FR-A3YO-06exon_skip_147024
89345480893520578934948189349481Nonsense_MutationCAp.E1157X
THYMTCGA-XU-A92Q-01exon_skip_147024
89345480893520578934960889349608Nonsense_MutationGTp.Y1114X
UCECTCGA-AX-A05Z-01exon_skip_147024
89345480893520578934979989349799Nonsense_MutationCAp.E1051*
BLCATCGA-DK-AA6W-01exon_skip_147024
89345480893520578935017789350177Nonsense_MutationCAp.E925*
HNSCTCGA-T2-A6WX-01exon_skip_147024
89345480893520578935023489350234Nonsense_MutationGAp.R906*
HNSCTCGA-CV-5440-01exon_skip_147024
89345480893520578935064489350644Nonsense_MutationGCp.S769*
HNSCTCGA-T2-A6X2-01exon_skip_147024
89345480893520578935064489350644Nonsense_MutationGCp.S769*
STADTCGA-HU-A4GU-01exon_skip_147024
89345480893520578935114989351149Nonsense_MutationGAp.R601*
STADTCGA-HU-A4GU-01exon_skip_147024
89345480893520578935114989351149Nonsense_MutationGAp.R601X
UCECTCGA-AP-A052-01exon_skip_147024
89345480893520578935118789351187Nonsense_MutationGTp.S588*
BLCATCGA-FD-A3B6-01exon_skip_147024
89345480893520578935172789351727Nonsense_MutationGCp.S408*

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description
ANKRD11_89341500_89341599_89345479_89352057_89352446_89352594_TCGA-HU-A4GU-01Sample: TCGA-HU-A4GU-01
Cancer type: STAD
ESID: exon_skip_147024
Skipped exon start: 89345480
Skipped exon end: 89352057
Mutation start: 89351149
Mutation end: 89351149
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: A
AAchange: p.R601X
ANKRD11_89341500_89341599_89345479_89352057_89352446_89352594_TCGA-HU-A4GU-01Sample: TCGA-HU-A4GU-01
Cancer type: STAD
ESID: exon_skip_147024
Skipped exon start: 89345480
Skipped exon end: 89352057
Mutation start: 89351149
Mutation end: 89351149
Mutation type: Nonsense_Mutation
Reference seq: G
Mutation seq: A
AAchange: p.R601*
exon_skip_109771_STAD_TCGA-HU-A4GU-01.png
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exon_skip_133402_STAD_TCGA-HU-A4GU-01.png
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exon_skip_133403_STAD_TCGA-HU-A4GU-01.png
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exon_skip_146776_STAD_TCGA-HU-A4GU-01.png
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exon_skip_147024_STAD_TCGA-HU-A4GU-01.png
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exon_skip_149455_STAD_TCGA-HU-A4GU-01.png
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exon_skip_335090_STAD_TCGA-HU-A4GU-01.png
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exon_skip_382354_STAD_TCGA-HU-A4GU-01.png
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exon_skip_433982_STAD_TCGA-HU-A4GU-01.png
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exon_skip_433985_STAD_TCGA-HU-A4GU-01.png
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exon_skip_437417_STAD_TCGA-HU-A4GU-01.png
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exon_skip_437418_STAD_TCGA-HU-A4GU-01.png
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exon_skip_454428_STAD_TCGA-HU-A4GU-01.png
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exon_skip_454431_STAD_TCGA-HU-A4GU-01.png
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exon_skip_454433_STAD_TCGA-HU-A4GU-01.png
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exon_skip_465824_STAD_TCGA-HU-A4GU-01.png
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exon_skip_467518_STAD_TCGA-HU-A4GU-01.png
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exon_skip_480057_STAD_TCGA-HU-A4GU-01.png
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exon_skip_485377_STAD_TCGA-HU-A4GU-01.png
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exon_skip_500520_STAD_TCGA-HU-A4GU-01.png
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ANKRD11_89341500_89341599_89345479_89352057_89352446_89352594_TCGA-L5-A4OI-01Sample: TCGA-L5-A4OI-01
Cancer type: ESCA
ESID: exon_skip_147024
Skipped exon start: 89345480
Skipped exon end: 89352057
Mutation start: 89349640
Mutation end: 89349641
Mutation type: Frame_Shift_Ins
Reference seq: -
Mutation seq: T
AAchange: p.*1104fs
ANKRD11_89341500_89341599_89345479_89352057_89352446_89352594_TCGA-L5-A4OI-01Sample: TCGA-L5-A4OI-01
Cancer type: ESCA
ESID: exon_skip_147024
Skipped exon start: 89345480
Skipped exon end: 89352057
Mutation start: 89349640
Mutation end: 89349641
Mutation type: Frame_Shift_Ins
Reference seq: -
Mutation seq: T
AAchange: p.D1103fs
exon_skip_112640_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_112965_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_122690_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_129706_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_135696_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_135704_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_135820_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_147024_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_149455_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_307491_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_308211_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_308974_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_309972_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_311841_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_328488_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_349475_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_352933_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_374468_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_374469_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_386802_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_423582_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_428975_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_434375_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_439047_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_439048_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_441654_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_443160_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_443161_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_457940_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_461524_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_470470_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_470694_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_474097_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_477308_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_487634_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_495456_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_502537_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_506535_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_55351_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_77217_ESCA_TCGA-L5-A4OI-01.png
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exon_skip_91288_ESCA_TCGA-L5-A4OI-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
RKO_LARGE_INTESTINE89345480893520578934588889345888Frame_Shift_DelG-p.P2354fs
SNUC4_LARGE_INTESTINE89345480893520578934615889346158Frame_Shift_DelG-p.P2264fs
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934643789346437Frame_Shift_DelG-p.P2171fs
HEC108_ENDOMETRIUM89345480893520578934799189347991Frame_Shift_DelC-p.K1653fs
OC316_OVARY89345480893520578934964189349641Frame_Shift_DelT-p.K1103fs
HEC59_ENDOMETRIUM89345480893520578934964189349641Frame_Shift_DelT-p.K1103fs
MHHPREB1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934964189349641Frame_Shift_DelT-p.K1103fs
OC314_OVARY89345480893520578934964189349641Frame_Shift_DelT-p.K1103fs
SHP77_LUNG89345480893520578934969089349691Frame_Shift_DelTT-p.K1087fs
HCT116_LARGE_INTESTINE89345480893520578935086289350862Frame_Shift_DelT-p.K696fs
MTA_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934615789346158Frame_Shift_Ins-Gp.A2265fs
A2780_OVARY89345480893520578934649689346497Frame_Shift_Ins-Tp.E2152fs
FEPD_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934865789348658Frame_Shift_Ins-Tp.N1431fs
MFE319_ENDOMETRIUM89345480893520578934964089349641Frame_Shift_Ins-Tp.D1104fs
SW48_LARGE_INTESTINE89345480893520578935105689351057Frame_Shift_Ins-Tp.H632fs
42MGBA_CENTRAL_NERVOUS_SYSTEM89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
A253_SALIVARY_GLAND89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
A704_KIDNEY89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
CAL148_BREAST89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
HS822T_FIBROBLAST89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
HSC4_UPPER_AERODIGESTIVE_TRACT89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
HUT102_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
ISTMES2_PLEURA89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
JHUEM1_ENDOMETRIUM89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
JHUEM7_ENDOMETRIUM89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
KE39_STOMACH89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
KMS21BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
KPNSI9S_AUTONOMIC_GANGLIA89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
NCIH1876_LUNG89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
NCIH810_LUNG89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
OCIM1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
SF172_CENTRAL_NERVOUS_SYSTEM89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
SH10TC_STOMACH89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
SKNMC_BONE89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
SW48_LARGE_INTESTINE89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
TIG3TD_FIBROBLAST89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
U251MG_CENTRAL_NERVOUS_SYSTEM89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
WM1799_SKIN89345480893520578935159489351595Frame_Shift_Ins-Tp.N452fs
SNU119_OVARY89345480893520578934952689349549In_Frame_DelCGCTGGCCTCTCCCATCTTGAACC-p.GFKMGEAS1134del
DOV13_OVARY89345480893520578935057489350576In_Frame_DelCTC-p.E792del
HS294T_SKIN89345480893520578935057489350576In_Frame_DelCTC-p.E792del
NCIH211_LUNG89337225893373178933723689337236Missense_MutationCTp.D2599N
COLO741_SKIN89337225893373178933729389337293Missense_MutationCTp.D2580N
SNU1040_LARGE_INTESTINE89337225893373178933729689337296Missense_MutationGAp.R2579C
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89337225893373178933731489337314Missense_MutationCTp.D2573N
HEC151_ENDOMETRIUM89341501893415998934150389341503Missense_MutationGAp.R2523W
DOTC24510_CERVIX89341501893415998934154989341549Missense_MutationCGp.Q2507H
HEC59_ENDOMETRIUM89345480893520578934553089345530Missense_MutationCTp.G2474S
JHUEM7_ENDOMETRIUM89345480893520578934554889345548Missense_MutationCTp.E2468K
KP3_PANCREAS89345480893520578934563789345637Missense_MutationTCp.Y2438C
KM12_LARGE_INTESTINE89345480893520578934568889345688Missense_MutationGAp.A2421V
5637_URINARY_TRACT89345480893520578934582989345829Missense_MutationGCp.S2374C
HCC202_BREAST89345480893520578934586389345863Missense_MutationGCp.P2363A
HCC2450_LUNG89345480893520578934588689345886Missense_MutationGAp.S2355F
SNU1040_LARGE_INTESTINE89345480893520578934598289345982Missense_MutationGAp.A2323V
HEC6_ENDOMETRIUM89345480893520578934600989346009Missense_MutationGAp.A2314V
NCIH1792_LUNG89345480893520578934604089346040Missense_MutationCTp.E2304K
SNUC4_LARGE_INTESTINE89345480893520578934605289346052Missense_MutationCTp.A2300T
639V_URINARY_TRACT89345480893520578934607389346073Missense_MutationCTp.D2293N
LK2_LUNG89345480893520578934607689346076Missense_MutationCAp.D2292Y
MOLM13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934609089346090Missense_MutationCTp.G2287D
SNU503_LARGE_INTESTINE89345480893520578934609089346090Missense_MutationCAp.G2287V
NCIH740_LUNG89345480893520578934609789346097Missense_MutationCAp.A2285S
SNU81_LARGE_INTESTINE89345480893520578934609789346097Missense_MutationCTp.A2285T
697_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934613289346132Missense_MutationCGp.G2273A
SW48_LARGE_INTESTINE89345480893520578934613389346133Missense_MutationCTp.G2273S
BT474_BREAST89345480893520578934617589346175Missense_MutationCTp.E2259K
MOLT16_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934623589346235Missense_MutationCTp.V2239M
NCIH513_PLEURA89345480893520578934625689346256Missense_MutationGAp.R2232C
KPNRTBM1_AUTONOMIC_GANGLIA89345480893520578934630389346303Missense_MutationGAp.A2216V
SNGM_ENDOMETRIUM89345480893520578934642489346424Missense_MutationCTp.G2176S
UWB1289_OVARY89345480893520578934645089346450Missense_MutationGAp.P2167L
SNU1066_UPPER_AERODIGESTIVE_TRACT89345480893520578934645789346457Missense_MutationCGp.E2165Q
SLR25_KIDNEY89345480893520578934647689346476Missense_MutationTGp.E2158D
EBC1_LUNG89345480893520578934648989346489Missense_MutationTGp.E2154A
KPNYN_AUTONOMIC_GANGLIA89345480893520578934648989346489Missense_MutationTGp.E2154A
LNCAPCLONEFGC_PROSTATE89345480893520578934650489346504Missense_MutationGAp.A2149V
SNU1040_LARGE_INTESTINE89345480893520578934650589346505Missense_MutationCTp.A2149T
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934651889346518Missense_MutationCAp.Q2144H
ISTMES1_PLEURA89345480893520578934652589346525Missense_MutationGAp.P2142L
SNU1040_LARGE_INTESTINE89345480893520578934653489346534Missense_MutationGAp.P2139L
639V_URINARY_TRACT89345480893520578934661389346613Missense_MutationCTp.G2113S
SW684_SOFT_TISSUE89345480893520578934662189346621Missense_MutationGAp.S2110F
SW1271_LUNG89345480893520578934663789346637Missense_MutationCAp.G2105C
COLO668_LUNG89345480893520578934668889346688Missense_MutationCTp.A2088T
MHHCALL3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934672689346726Missense_MutationGAp.A2075V
TGBC11TKB_STOMACH89345480893520578934673289346732Missense_MutationGAp.P2073L
LNCAPCLONEFGC_PROSTATE89345480893520578934675189346751Missense_MutationTCp.S2067G
S117_SOFT_TISSUE89345480893520578934679889346798Missense_MutationGAp.S2051L
HEC59_ENDOMETRIUM89345480893520578934681489346814Missense_MutationCTp.A2046T
22RV1_PROSTATE89345480893520578934686289346862Missense_MutationCTp.A2030T
PACADD119_PANCREAS89345480893520578934689789346897Missense_MutationGAp.P2018L
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934696089346960Missense_MutationGAp.A1997V
HEC108_ENDOMETRIUM89345480893520578934696189346961Missense_MutationCTp.A1997T
C4I_CERVIX89345480893520578934696889346968Missense_MutationGTp.F1994L
RH30_SOFT_TISSUE89345480893520578934703289347032Missense_MutationCAp.W1973L
SJRH30_SOFT_TISSUE89345480893520578934703289347032Missense_MutationCAp.W1973L
NCIH1299_LUNG89345480893520578934714589347145Missense_MutationGCp.D1935E
AGS_STOMACH89345480893520578934714989347149Missense_MutationAGp.L1934P
MHHES1_BONE89345480893520578934724989347249Missense_MutationGAp.P1901S
COLO800_SKIN89345480893520578934724989347249Missense_MutationGAp.P1901S
SNU119_OVARY89345480893520578934727089347270Missense_MutationGTp.P1894T
SNU1040_LARGE_INTESTINE89345480893520578934737789347377Missense_MutationGAp.P1858L
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934737889347378Missense_MutationGAp.P1858S
8305C_THYROID89345480893520578934739389347393Missense_MutationGCp.P1853A
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934743189347431Missense_MutationGAp.A1840V
K2_SKIN89345480893520578934743589347435Missense_MutationGAp.P1839S
MCC13_SKIN89345480893520578934745989347459Missense_MutationCAp.D1831Y
TE6_OESOPHAGUS89345480893520578934754389347543Missense_MutationAGp.F1803L
K562_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934755289347552Missense_MutationCTp.E1800K
RH18_SOFT_TISSUE89345480893520578934761589347615Missense_MutationGAp.P1779S
HCT116_LARGE_INTESTINE89345480893520578934772089347720Missense_MutationGAp.H1744Y
NCIH2052_PLEURA89345480893520578934773789347737Missense_MutationTCp.D1738G
LNCAPCLONEFGC_PROSTATE89345480893520578934775889347758Missense_MutationTAp.D1731V
FADU_UPPER_AERODIGESTIVE_TRACT89345480893520578934775889347758Missense_MutationTCp.D1731G
HEC1A_ENDOMETRIUM89345480893520578934776589347765Missense_MutationCTp.A1729T
HEC1_ENDOMETRIUM89345480893520578934776589347765Missense_MutationCTp.A1729T
HEC1B_ENDOMETRIUM89345480893520578934776589347765Missense_MutationCTp.A1729T
OC316_OVARY89345480893520578934782789347827Missense_MutationGAp.S1708L
OC314_OVARY89345480893520578934782789347827Missense_MutationGAp.S1708L
NCIH2882_LUNG89345480893520578934783089347830Missense_MutationGAp.T1707M
UPCISCC152_UPPER_AERODIGESTIVE_TRACT89345480893520578934785489347854Missense_MutationCTp.R1699Q
RKO_LARGE_INTESTINE89345480893520578934785489347854Missense_MutationCTp.R1699Q
SCC90_UPPER_AERODIGESTIVE_TRACT89345480893520578934785489347854Missense_MutationCTp.R1699Q
MEWO_SKIN89345480893520578934785589347855Missense_MutationGAp.R1699W
MEWO_SKIN89345480893520578934785589347857Missense_MutationGGCAAAp.1698_1699SR>IW
MEWO_SKIN89345480893520578934785789347857Missense_MutationCAp.S1698I
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934787689347876Missense_MutationATp.S1692T
SNU398_LIVER89345480893520578934789589347895Missense_MutationCTp.M1685I
HGC27_STOMACH89345480893520578934790389347903Missense_MutationGAp.P1683S
SNU520_STOMACH89345480893520578934790589347905Missense_MutationCTp.G1682D
NCIH2081_LUNG89345480893520578934794789347947Missense_MutationATp.L1668Q
HCT116_LARGE_INTESTINE89345480893520578934806289348062Missense_MutationCTp.G1630R
KELLY_AUTONOMIC_GANGLIA89345480893520578934810989348109Missense_MutationCTp.R1614Q
HCT15_LARGE_INTESTINE89345480893520578934815289348152Missense_MutationGAp.R1600W
SNU1040_LARGE_INTESTINE89345480893520578934816189348161Missense_MutationGAp.R1597C
NCIH292_LUNG89345480893520578934828089348280Missense_MutationGTp.P1557Q
CCRFCEM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934829989348299Missense_MutationCTp.G1551R
SW403_LARGE_INTESTINE89345480893520578934835489348354Missense_MutationCAp.E1532D
SNU407_LARGE_INTESTINE89345480893520578934838989348389Missense_MutationCTp.E1521K
SNU175_LARGE_INTESTINE89345480893520578934841389348413Missense_MutationCTp.V1513M
SNU1040_LARGE_INTESTINE89345480893520578934841989348419Missense_MutationGAp.P1511S
PF382_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934847089348470Missense_MutationGAp.R1494W
LI7_LIVER89345480893520578934854389348543Missense_MutationCGp.W1469C
DSH1_URINARY_TRACT89345480893520578934855489348554Missense_MutationTCp.R1466G
CAL120_BREAST89345480893520578934856889348568Missense_MutationTCp.K1461R
EB2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934865889348658Missense_MutationTGp.N1431T
COV434_OVARY89345480893520578934881889348818Missense_MutationCTp.E1378K
HCT116_LARGE_INTESTINE89345480893520578934893489348934Missense_MutationCTp.C1339Y
NCIH2286_LUNG89345480893520578934895689348956Missense_MutationCTp.D1332N
EFO27_OVARY89345480893520578934899489348994Missense_MutationGAp.A1319V
CTV1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934900489349004Missense_MutationCAp.G1316W
EW16_BONE89345480893520578934907389349073Missense_MutationTCp.R1293G
KE37_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934913889349138Missense_MutationGCp.S1271W
ZR751_BREAST89345480893520578934916989349169Missense_MutationCGp.D1261H
YMB1E_BREAST89345480893520578934916989349169Missense_MutationCGp.D1261H
DMS53_LUNG89345480893520578934922789349227Missense_MutationCGp.K1241N
ZR751_BREAST89345480893520578934934389349343Missense_MutationCGp.E1203Q
YMB1E_BREAST89345480893520578934934389349343Missense_MutationCGp.E1203Q
SNGM_ENDOMETRIUM89345480893520578934941989349419Missense_MutationCAp.K1177N
PC9_LUNG89345480893520578934942489349424Missense_MutationGTp.Q1176K
PC14_LUNG89345480893520578934942489349424Missense_MutationGTp.Q1176K
ANGMCSS_CENTRAL_NERVOUS_SYSTEM89345480893520578934950889349508Missense_MutationCTp.G1148S
M980513_SKIN89345480893520578934952989349529Missense_MutationTCp.S1141G
CHP126_AUTONOMIC_GANGLIA89345480893520578934965289349652Missense_MutationAGp.S1100P
GBM001_CENTRAL_NERVOUS_SYSTEM89345480893520578934967689349676Missense_MutationGAp.P1092S
EW12_BONE89345480893520578934967689349676Missense_MutationGAp.P1092S
MET2B89345480893520578934972989349729Missense_MutationTGp.K1074T
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934973089349730Missense_MutationTCp.K1074E
DOTC24510_CERVIX89345480893520578934989889349898Missense_MutationCGp.E1018Q
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934994689349946Missense_MutationGAp.R1002W
JHOS4_OVARY89345480893520578934995489349954Missense_MutationGAp.P999L
SF126_CENTRAL_NERVOUS_SYSTEM89345480893520578934995489349954Missense_MutationGAp.P999L
HCET_UPPER_AERODIGESTIVE_TRACT89345480893520578934995489349954Missense_MutationGAp.P999L
ESS1_ENDOMETRIUM89345480893520578934997889349978Missense_MutationCTp.G991D
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934999189349991Missense_MutationCAp.D987Y
DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935000389350003Missense_MutationTCp.S983G
639V_URINARY_TRACT89345480893520578935004589350045Missense_MutationCTp.E969K
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935005489350054Missense_MutationCTp.A966T
HEC1_ENDOMETRIUM89345480893520578935006589350065Missense_MutationCAp.R962M
LAMA84_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935006889350068Missense_MutationCAp.R961L
SKNO1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935016789350167Missense_MutationTGp.K928T
KYSE410_OESOPHAGUS89345480893520578935017989350179Missense_MutationGCp.T924S
SKM1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935018189350181Missense_MutationCAp.Q923H
LAN6_AUTONOMIC_GANGLIA89345480893520578935028189350281Missense_MutationCTp.R890Q
P30OHK_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935034789350347Missense_MutationAGp.M868T
HEC108_ENDOMETRIUM89345480893520578935035389350353Missense_MutationCAp.R866M
SNU182_LIVER89345480893520578935043289350432Missense_MutationGAp.R840W
SNU81_LARGE_INTESTINE89345480893520578935043289350432Missense_MutationGAp.R840W
TTC466_BONE89345480893520578935044489350444Missense_MutationCTp.D836N
HEC251_ENDOMETRIUM89345480893520578935046189350461Missense_MutationTGp.K830T
HCC1954_BREAST89345480893520578935048489350484Missense_MutationCGp.Q822H
HCC1954_MATCHED_NORMAL_TISSUE89345480893520578935048489350484Missense_MutationCGp.Q822H
OCILY132_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935052589350525Missense_MutationTAp.R809W
MERO84_LUNG89345480893520578935054589350545Missense_MutationACp.L802R
CHLA218_BONE89345480893520578935056989350569Missense_MutationAGp.I794T
CORL303_LUNG89345480893520578935073789350737Missense_MutationCTp.R738H
A3KAW_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935075289350752Missense_MutationCTp.R733Q
HCC2450_LUNG89345480893520578935075889350758Missense_MutationGCp.S731C
DIPG007_CENTRAL_NERVOUS_SYSTEM89345480893520578935086689350866Missense_MutationTAp.K695I
LOVO_LARGE_INTESTINE89345480893520578935093289350932Missense_MutationAGp.L673P
OVCAR5_OVARY89345480893520578935107589351075Missense_MutationCGp.E625D
NCIH820_LUNG89345480893520578935120889351208Missense_MutationGAp.S581F
L540_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935122489351224Missense_MutationCTp.E576K
DIPG007_CENTRAL_NERVOUS_SYSTEM89345480893520578935135889351358Missense_MutationGAp.A531V
LN319_CENTRAL_NERVOUS_SYSTEM89345480893520578935137989351379Missense_MutationGAp.S524L
D542MG_CENTRAL_NERVOUS_SYSTEM89345480893520578935138989351389Missense_MutationACp.S521A
L542_MATCHED_NORMAL_TISSUE89345480893520578935138989351389Missense_MutationACp.S521A
JHH6_LIVER89345480893520578935139489351394Missense_MutationGAp.S519F
OCILY132_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935146889351468Missense_MutationGCp.D494E
HEC1_ENDOMETRIUM89345480893520578935155289351552Missense_MutationCAp.E466D
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935173689351736Missense_MutationCTp.R405H
NALM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935176389351763Missense_MutationGAp.T396M
CW2_LARGE_INTESTINE89345480893520578935177289351772Missense_MutationTCp.K393R
SCC3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935178889351788Missense_MutationCGp.V388L
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935187189351871Missense_MutationGAp.P360L
OVTOKO_OVARY89345480893520578935194589351945Missense_MutationCGp.E335D
SNU1076_UPPER_AERODIGESTIVE_TRACT89345480893520578935205489352054Missense_MutationCTp.S299N
CW2_LARGE_INTESTINE89371614893717528937174689371746Missense_MutationCAp.D32Y
RERFLCFM_LUNG89371614893717528937174989371749Missense_MutationTCp.K31E
SKGT4_OESOPHAGUS89383341893834838938337089383370Missense_MutationCTp.D20N
SKGT4_OESOPHAGUS89383341893834868938337089383370Missense_MutationCTp.D20N
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934575889345758Nonsense_MutationGAp.Q2398*
CL34_LARGE_INTESTINE89345480893520578934720789347207Nonsense_MutationCAp.E1915*
HDQP1_BREAST89345480893520578934729989347299Nonsense_MutationGCp.S1884*
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934818589348185Nonsense_MutationGAp.Q1589*
PC9_LUNG89345480893520578934956089349560Nonsense_MutationGTp.C1130*
PC14_LUNG89345480893520578934956089349560Nonsense_MutationGTp.C1130*
8305C_THYROID89345480893520578934986689349866Nonsense_MutationGCp.Y1028*
KNS62_LUNG89345480893520578934989889349898Nonsense_MutationCAp.E1018*
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578934993189349931Nonsense_MutationGAp.R1007*
SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935023489350234Nonsense_MutationGAp.R906*
IPC298_SKIN89345480893520578935048689350486Nonsense_MutationGAp.Q822*
HEC251_ENDOMETRIUM89345480893520578935064489350644Nonsense_MutationGTp.S769*
HEP3B217_LIVER89345480893520578935082089350820Nonsense_MutationCTp.W710*
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935114989351149Nonsense_MutationGAp.R601*
KHYG_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE89345480893520578935157889351578Nonsense_MutationGAp.R458*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ANKRD11

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 ANKRD11


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ANKRD11


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RelatedDrugs for ANKRD11

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 ANKRD11

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
ANKRD11C0005944Metabolic Bone Disorder1CTD_human
ANKRD11C1510586Autism Spectrum Disorders1CTD_human