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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 TRIP11

check button Gene summary
Gene informationGene symbol

TRIP11

Gene ID

9321

Gene namethyroid hormone receptor interactor 11
SynonymsACG1A|CEV14|GMAP-210|GMAP210|TRIP-11|TRIP230
Cytomap

14q32.12

Type of geneprotein-coding
Descriptionthyroid receptor-interacting protein 11Golgi-microtubule-associated protein of 210 kDaTR-interacting protein 11clonal evolution-related gene on chromosome 14 proteingolgi-associated microtubule-binding protein 210
Modification date20180522
UniProtAcc

Q15643

ContextPubMed: TRIP11 [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 TRIP11 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 TRIP11

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 TRIP11

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1151831492439060:92439205:92440970:92441087:92441515:9244163092440970:92441087ENSG00000100815.8ENST00000554357.1,ENST00000267622.4
exon_skip_1151861492440970:92441087:92441515:92441630:92442451:9244253392441515:92441630ENSG00000100815.8ENST00000554357.1,ENST00000267622.4
exon_skip_1151871492441515:92441630:92442451:92442533:92454627:9245472792442451:92442533ENSG00000100815.8ENST00000554357.1,ENST00000267622.4
exon_skip_1151881492442451:92442533:92443469:92443592:92454627:9245472792443469:92443592ENSG00000100815.8ENST00000557017.1
exon_skip_1151891492460152:92460256:92461695:92461859:92465583:9246572392461695:92461859ENSG00000100815.8ENST00000554357.1,ENST00000267622.4,ENST00000557017.1
exon_skip_1151901492466311:92466452:92469762:92472792:92473983:9247419692469762:92472792ENSG00000100815.8ENST00000554357.1,ENST00000267622.4
exon_skip_1151911492473983:92474196:92477329:92477416:92478098:9247813992477329:92477416ENSG00000100815.8ENST00000267622.4
exon_skip_1151931492473983:92474196:92478098:92478139:92480558:9248092192478098:92478139ENSG00000100815.8ENST00000554357.1
exon_skip_1151941492477329:92477416:92478098:92478139:92480558:9248092192478098:92478139ENSG00000100815.8ENST00000267622.4
exon_skip_1151961492482176:92482205:92484025:92484094:92487899:9248817592484025:92484094ENSG00000100815.8ENST00000555516.2,ENST00000267622.4
exon_skip_1151971492484025:92484094:92487899:92488175:92491653:9249176492487899:92488175ENSG00000100815.8ENST00000555516.2,ENST00000267622.4

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

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Exon skipping events with PSIs in GTEx for TRIP11

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_1151831492439060:92439205:92440970:92441087:92441515:9244163092440970:92441087ENSG00000100815.8ENST00000267622.4,ENST00000554357.1
exon_skip_1151861492440970:92441087:92441515:92441630:92442451:9244253392441515:92441630ENSG00000100815.8ENST00000267622.4,ENST00000554357.1
exon_skip_1151871492441515:92441630:92442451:92442533:92454627:9245472792442451:92442533ENSG00000100815.8ENST00000267622.4,ENST00000554357.1
exon_skip_1151881492442451:92442533:92443469:92443592:92454627:9245472792443469:92443592ENSG00000100815.8ENST00000557017.1
exon_skip_1151891492460152:92460256:92461695:92461859:92465583:9246572392461695:92461859ENSG00000100815.8ENST00000267622.4,ENST00000554357.1,ENST00000557017.1
exon_skip_1151901492466311:92466452:92469762:92472792:92473983:9247419692469762:92472792ENSG00000100815.8ENST00000267622.4,ENST00000554357.1
exon_skip_1151911492473983:92474196:92477329:92477416:92478098:9247813992477329:92477416ENSG00000100815.8ENST00000267622.4
exon_skip_1151931492473983:92474196:92478098:92478139:92480558:9248092192478098:92478139ENSG00000100815.8ENST00000554357.1
exon_skip_1151941492477329:92477416:92478098:92478139:92480558:9248092192478098:92478139ENSG00000100815.8ENST00000267622.4
exon_skip_1151971492484025:92484094:92487899:92488175:92491653:9249176492487899:92488175ENSG00000100815.8ENST00000267622.4,ENST00000555516.2

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 TRIP11

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
ENST000002676229244151592441630Frame-shift
ENST000002676229244245192442533Frame-shift
ENST000002676229246169592461859Frame-shift
ENST000002676229247809892478139Frame-shift
ENST000002676229244097092441087In-frame
ENST000002676229246976292472792In-frame
ENST000002676229247732992477416In-frame
ENST000002676229248402592484094In-frame
ENST000002676229248789992488175In-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
ENST000002676229244151592441630Frame-shift
ENST000002676229244245192442533Frame-shift
ENST000002676229246169592461859Frame-shift
ENST000002676229247809892478139Frame-shift
ENST000002676229244097092441087In-frame
ENST000002676229246976292472792In-frame
ENST000002676229247732992477416In-frame
ENST000002676229248789992488175In-frame

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Infer the effects of exon skipping event on protein functional features for TRIP11

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
ENST000002676221001319799248789992488175687962104196
ENST0000026762210013197992484025924840949631031196219
ENST00000267622100131979924773299247741616021688409438
ENST000002676221001319799246976292472792190249315091519
ENST0000026762210013197992440970924410875832594818191858

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
ENST000002676221001319799248789992488175687962104196
ENST00000267622100131979924773299247741616021688409438
ENST000002676221001319799246976292472792190249315091519
ENST0000026762210013197992440970924410875832594818191858

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
Q1564310419621979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q15643104196521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q15643104196121121Sequence conflictNote=L->F;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q1564319621921979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q15643196219521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q1564340943821979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q15643409438521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q15643509151921979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q156435091519521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q156435091519559559Natural variantID=VAR_079175;Note=V->A;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:27717682;Dbxref=PMID:27717682
Q156435091519795795Natural variantID=VAR_055863;Note=V->L;Dbxref=dbSNP:rs34699762
Q156435091519884884Natural variantID=VAR_055864;Note=D->G;Dbxref=dbSNP:rs34967261
Q15643509151910401040Natural variantID=VAR_055865;Note=I->V;Dbxref=dbSNP:rs34805848
Q15643509151911071107Natural variantID=VAR_060344;Note=E->D;Dbxref=dbSNP:rs4619320
Q15643509151914131413Natural variantID=VAR_060345;Note=D->A;Dbxref=dbSNP:rs12884523
Q15643509151915031503Natural variantID=VAR_055866;Note=M->V;Dbxref=dbSNP:rs34839498
Q156435091519516516Sequence conflictNote=D->A;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q156435091519561563Sequence conflictNote=KEK->FVL;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151912021202Sequence conflictNote=N->H;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151912371237Sequence conflictNote=H->R;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151913461347Sequence conflictNote=QQ->HE;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q156431819185821979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q156431819185817741823DomainNote=GRIP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00250
Q156431819185818421842Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:19690332,ECO:0000244|PubMed:20068231;Dbxref=PMID:18669648,PMID:19690332,PMID:20068231
Q156431819185818461846Modified residueNote=Phosphothreonine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:19690332;Dbxref=PMID:18669648,PMID:19690332
Q156431819185818271827Natural variantID=VAR_060346;Note=G->S;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:10189370,ECO:0000269|PubMed:15489334,ECO:0000269|PubMed:7776974,ECO:0000269|PubMed:9373237;Dbxref=dbSNP:rs1051340,PMID:10189370,PMID:15489334
Q156431819185818461846Natural variantID=VAR_054151;Note=T->I;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18987736;Dbxref=dbSNP:rs141259390,PMID:18987736


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
Q1564310419621979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q15643104196521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q15643104196121121Sequence conflictNote=L->F;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q1564340943821979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q15643409438521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q15643509151921979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q156435091519521773Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q156435091519559559Natural variantID=VAR_079175;Note=V->A;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:27717682;Dbxref=PMID:27717682
Q156435091519795795Natural variantID=VAR_055863;Note=V->L;Dbxref=dbSNP:rs34699762
Q156435091519884884Natural variantID=VAR_055864;Note=D->G;Dbxref=dbSNP:rs34967261
Q15643509151910401040Natural variantID=VAR_055865;Note=I->V;Dbxref=dbSNP:rs34805848
Q15643509151911071107Natural variantID=VAR_060344;Note=E->D;Dbxref=dbSNP:rs4619320
Q15643509151914131413Natural variantID=VAR_060345;Note=D->A;Dbxref=dbSNP:rs12884523
Q15643509151915031503Natural variantID=VAR_055866;Note=M->V;Dbxref=dbSNP:rs34839498
Q156435091519516516Sequence conflictNote=D->A;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q156435091519561563Sequence conflictNote=KEK->FVL;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151912021202Sequence conflictNote=N->H;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151912371237Sequence conflictNote=H->R;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q15643509151913461347Sequence conflictNote=QQ->HE;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q156431819185821979ChainID=PRO_0000190076;Note=Thyroid receptor-interacting protein 11
Q156431819185817741823DomainNote=GRIP;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00250
Q156431819185818421842Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244,ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:19690332,ECO:0000244|PubMed:20068231;Dbxref=PMID:18669648,PMID:19690332,PMID:20068231
Q156431819185818461846Modified residueNote=Phosphothreonine;Ontology_term=ECO:0000244,ECO:0000244;evidence=ECO:0000244|PubMed:18669648,ECO:0000244|PubMed:19690332;Dbxref=PMID:18669648,PMID:19690332
Q156431819185818271827Natural variantID=VAR_060346;Note=G->S;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:10189370,ECO:0000269|PubMed:15489334,ECO:0000269|PubMed:7776974,ECO:0000269|PubMed:9373237;Dbxref=dbSNP:rs1051340,PMID:10189370,PMID:15489334
Q156431819185818461846Natural variantID=VAR_054151;Note=T->I;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:18987736;Dbxref=dbSNP:rs141259390,PMID:18987736


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SNVs in the skipped exons for TRIP11

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

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

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
LIHCTCGA-DD-A39Y-01exon_skip_115183
92440971924410879244102192441021Frame_Shift_DelT-p.S1842fs
LIHCTCGA-DD-A3A0-01exon_skip_115183
92440971924410879244102192441021Frame_Shift_DelT-p.S1842fs
LIHCTCGA-G3-A3CJ-01exon_skip_115186
92441516924416309244155292441552Frame_Shift_DelC-p.G1807fs
LIHCTCGA-DD-A3A0-01exon_skip_115190
92469763924727929246985292469852Frame_Shift_DelA-p.S1490fs
LIHCTCGA-G3-A3CJ-01exon_skip_115190
92469763924727929246985292469852Frame_Shift_DelA-p.S1490fs
LIHCTCGA-DD-A3A0-01exon_skip_115190
92469763924727929246991892469918Frame_Shift_DelT-p.I1468fs
LIHCTCGA-DD-A1EG-01exon_skip_115190
92469763924727929247010692470106Frame_Shift_DelA-p.L1405fs
LIHCTCGA-DD-A3A0-01exon_skip_115190
92469763924727929247043292470432Frame_Shift_DelC-p.G1296fs
LIHCTCGA-G3-A3CJ-01exon_skip_115190
92469763924727929247046592470465Frame_Shift_DelC-p.G1285fs
LIHCTCGA-DD-A1EG-01exon_skip_115190
92469763924727929247140992471409Frame_Shift_DelT-p.T971fs
LIHCTCGA-G3-A3CJ-01exon_skip_115190
92469763924727929247166192471661Frame_Shift_DelT-p.T887fs
LIHCTCGA-DD-A39Y-01exon_skip_115190
92469763924727929247185392471853Frame_Shift_DelT-p.R823fs
LIHCTCGA-DD-A39Y-01exon_skip_115190
92469763924727929247209692472096Frame_Shift_DelT-p.T742fs
LIHCTCGA-DD-A1EG-01exon_skip_115190
92469763924727929247217492472174Frame_Shift_DelT-p.M716fs
LIHCTCGA-DD-A39Y-01exon_skip_115190
92469763924727929247219792472197Frame_Shift_DelT-p.N708fs
LIHCTCGA-DD-A3A1-01exon_skip_115190
92469763924727929247220492472204Frame_Shift_DelC-p.E706fs
COADTCGA-CK-5913-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
COADTCGA-G4-6628-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
LIHCTCGA-G3-A3CJ-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
STADTCGA-BR-8368-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
STADTCGA-CG-5733-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
STADTCGA-HU-A4GQ-01exon_skip_115190
92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
LIHCTCGA-DD-A3A0-01exon_skip_115190
92469763924727929247275292472752Frame_Shift_DelT-p.N523fs
BLCATCGA-DK-A6AW-01exon_skip_115190
92469763924727929247139092471391Frame_Shift_Ins-Tp.T977fs
LIHCTCGA-ED-A8O6-01exon_skip_115190
92469763924727929247219692472197Frame_Shift_Ins-Tp.N708fs
READTCGA-EI-6507-01exon_skip_115189
92461696924618599246169692461696Nonsense_MutationCAp.E1686X
READTCGA-F5-6814-01exon_skip_115190
92469763924727929246984092469840Nonsense_MutationGAp.R1494X
UCECTCGA-B5-A11E-01exon_skip_115190
92469763924727929246984092469840Nonsense_MutationGAp.R1494*
CHOLTCGA-W5-AA2X-01exon_skip_115190
92469763924727929247047692470476Nonsense_MutationTAp.K1282*
CHOLTCGA-W5-AA2X-01exon_skip_115190
92469763924727929247047692470476Nonsense_MutationTAp.K1282X
COADTCGA-AZ-4315-01exon_skip_115190
92469763924727929247123892471238Nonsense_MutationGAp.R1028X
BLCATCGA-G2-A3IE-01exon_skip_115190
92469763924727929247133792471337Nonsense_MutationGAp.Q995*
SKCMTCGA-W3-AA1V-06exon_skip_115190
92469763924727929247133792471337Nonsense_MutationGAp.Q995*
LUADTCGA-78-7155-01exon_skip_115190
92469763924727929247170992471709Nonsense_MutationGAp.R871*
STADTCGA-VQ-A8P2-01exon_skip_115190
92469763924727929247243592472435Nonsense_MutationGAp.Q629*
STADTCGA-VQ-A8P2-01exon_skip_115190
92469763924727929247243592472435Nonsense_MutationGAp.Q629X
ESCATCGA-L5-A4OE-01exon_skip_115190
92469763924727929247250792472507Nonsense_MutationCAp.E605*
ESCATCGA-L5-A4OE-01exon_skip_115190
92469763924727929247250792472507Nonsense_MutationCAp.E605X

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

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
SNU407_LARGE_INTESTINE92469763924727929247037792470377Frame_Shift_DelG-p.Q1315fs
EW22_BONE92469763924727929247063092470636Frame_Shift_DelGGTCATC-p.VMT1228fs
SNUC2A_LARGE_INTESTINE92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
HCT116_LARGE_INTESTINE92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
FARAGE_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
SNUC2B_LARGE_INTESTINE92469763924727929247269892472698Frame_Shift_DelT-p.K541fs
DV90_LUNG92469763924727929247140892471409Frame_Shift_Ins-Tp.T971fs
HS616T_FIBROBLAST92440971924410879244100092441000Missense_MutationTCp.R1849G
CAL39_VULVA92440971924410879244100692441006Missense_MutationGTp.P1847T
TGBC11TKB_STOMACH92441516924416309244154792441547Missense_MutationATp.I1809N
DMS79_LUNG92461696924618599246177192461771Missense_MutationCAp.V1661F
NALM19_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929246987392469873Missense_MutationGCp.Q1483E
SNUC2A_LARGE_INTESTINE92469763924727929246987392469873Missense_MutationGCp.Q1483E
SNUC2B_LARGE_INTESTINE92469763924727929246987392469873Missense_MutationGCp.Q1483E
MOLT3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929246987892469878Missense_MutationGAp.A1481V
S117_SOFT_TISSUE92469763924727929246991792469917Missense_MutationACp.I1468R
HCC366_LUNG92469763924727929247002392470023Missense_MutationTCp.K1433E
MESSA_SOFT_TISSUE92469763924727929247006892470068Missense_MutationCGp.A1418P
HEC108_ENDOMETRIUM92469763924727929247010092470100Missense_MutationTCp.K1407R
SCC4_UPPER_AERODIGESTIVE_TRACT92469763924727929247014692470146Missense_MutationCAp.D1392Y
HEC108_ENDOMETRIUM92469763924727929247015792470157Missense_MutationTAp.H1388L
MDAMB361_BREAST92469763924727929247017092470170Missense_MutationCGp.E1384Q
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247023392470233Missense_MutationTCp.I1363V
HGC27_STOMACH92469763924727929247032292470322Missense_MutationCTp.S1333N
HCC38_BREAST92469763924727929247068192470681Missense_MutationCAp.K1213N
SW756_CERVIX92469763924727929247068692470686Missense_MutationCAp.D1212Y
PCM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247076692470766Missense_MutationGAp.A1185V
PLCPRF5_LIVER92469763924727929247078692470786Missense_MutationCGp.Q1178H
LS411N_LARGE_INTESTINE92469763924727929247085492470854Missense_MutationTCp.R1156G
HEC108_ENDOMETRIUM92469763924727929247086092470860Missense_MutationTCp.M1154V
JHU011_UPPER_AERODIGESTIVE_TRACT92469763924727929247086292470862Missense_MutationTCp.D1153G
KP4_PANCREAS92469763924727929247087792470877Missense_MutationTCp.E1148G
SUIT2_PANCREAS92469763924727929247089192470891Missense_MutationCAp.L1143F
HEC265_ENDOMETRIUM92469763924727929247089492470894Missense_MutationTAp.K1142N
HEC251_ENDOMETRIUM92469763924727929247091092470910Missense_MutationTCp.Q1137R
KMS12BM_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247091092470910Missense_MutationTCp.Q1137R
TE14_OESOPHAGUS92469763924727929247091092470910Missense_MutationTCp.Q1137R
SNU1272_KIDNEY92469763924727929247111192471111Missense_MutationGAp.A1070V
NCIH522_LUNG92469763924727929247123792471237Missense_MutationCTp.R1028Q
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247129192471291Missense_MutationTCp.K1010R
ECC10_STOMACH92469763924727929247138292471382Missense_MutationGCp.H980D
DOV13_OVARY92469763924727929247145692471456Missense_MutationGAp.T955I
JHH2_LIVER92469763924727929247145792471457Missense_MutationTCp.T955A
MOLT3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247163692471636Missense_MutationGAp.A895V
REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247168292471682Missense_MutationCTp.A880T
SNU1040_LARGE_INTESTINE92469763924727929247168292471682Missense_MutationCTp.A880T
HS751T_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247187892471878Missense_MutationTGp.E814D
JHUEM7_ENDOMETRIUM92469763924727929247189292471892Missense_MutationTGp.I810L
JHH5_LIVER92469763924727929247190792471908Missense_MutationGCTTp.Q805K
NB1_AUTONOMIC_GANGLIA92469763924727929247190792471908Missense_MutationGCTTp.Q805K
NB1_AUTONOMIC_GANGLIA92469763924727929247190792471907Missense_MutationGTp.Q805K
JHH5_LIVER92469763924727929247190792471907Missense_MutationGTp.Q805K
PLCPRF5_LIVER92469763924727929247201492472014Missense_MutationTGp.Q769P
HEC1A_ENDOMETRIUM92469763924727929247227992472279Missense_MutationTCp.K681E
HUNS1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92469763924727929247231692472316Missense_MutationTAp.L668F
NCIH513_PLEURA92469763924727929247232492472324Missense_MutationCTp.E666K
MFE319_ENDOMETRIUM92469763924727929247239092472390Missense_MutationGAp.L644F
MCC13_SKIN92469763924727929247254992472549Missense_MutationGCp.Q591E
HT115_LARGE_INTESTINE92469763924727929247256192472561Missense_MutationTGp.N587H
NCIH1770_LUNG92469763924727929247261192472611Missense_MutationGAp.A570V
NCIH2106_LUNG92469763924727929247261192472611Missense_MutationGAp.A570V
CALU1_LUNG92477330924774169247738092477380Missense_MutationTCp.M422V
ISHIKAWAHERAKLIO02ER_ENDOMETRIUM92478099924781399247811392478113Missense_MutationTGp.S405R
PECAPJ49_UPPER_AERODIGESTIVE_TRACT92484026924840949248403492484034Missense_MutationTCp.I217V
RCHACV_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92484026924840949248407392484073Missense_MutationCTp.D204N
SW684_SOFT_TISSUE92484026924840949248409092484090Missense_MutationGAp.S198F
SNU520_STOMACH92487900924881759248807092488070Missense_MutationTGp.T140P
KASUMI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92487900924881759248808292488082Missense_MutationCTp.G136S
CORL88_LUNG92461696924618599246183792461837Nonsense_MutationCAp.E1639*
SNU349_KIDNEY92461696924618599246184392461843Nonsense_MutationGAp.Q1637*
HEC1B_ENDOMETRIUM92469763924727929246984092469840Nonsense_MutationGAp.R1494*
HCC2450_LUNG92469763924727929247017892470178Nonsense_MutationGCp.S1381*
FTC238_THYROID92469763924727929247123892471238Nonsense_MutationGAp.R1028*
CORL32_LUNG92469763924727929247124192471241Nonsense_MutationCAp.E1027*
22RV1_PROSTATE92469763924727929247191392471913Nonsense_MutationGAp.Q803*
BCP1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE92487900924881759248795592487955Nonsense_MutationGCp.S178*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for TRIP11

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 TRIP11


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for TRIP11


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RelatedDrugs for TRIP11

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 TRIP11

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