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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 TPR

check button Gene summary
Gene informationGene symbol

TPR

Gene ID

7175

Gene nametranslocated promoter region, nuclear basket protein
Synonyms-
Cytomap

1q31.1

Type of geneprotein-coding
Descriptionnucleoprotein TPRNPC-associated intranuclear proteinmegatornuclear pore complex-associated protein TPRtranslocated promoter region (to activated MET oncogene)translocated promoter region proteintumor potentiating region
Modification date20180523
UniProtAcc

P12270

ContextPubMed: TPR [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
TPR

GO:0006404

RNA import into nucleus

9864356

TPR

GO:0006606

protein import into nucleus

9864356

TPR

GO:0031990

mRNA export from nucleus in response to heat stress

17897941

TPR

GO:0034605

cellular response to heat

17897941

TPR

GO:0046832

negative regulation of RNA export from nucleus

22253824

TPR

GO:0070849

response to epidermal growth factor

18794356


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Exon skipping events across known transcript of Ensembl for TPR 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 TPR

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 TPR

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_350921186280783:186283158:186283760:186283856:186286613:186286732186283760:186283856ENSG00000047410.9ENST00000367478.4
exon_skip_350951186283760:186283856:186286613:186286732:186287578:186287735186286613:186286732ENSG00000047410.9ENST00000367478.4
exon_skip_350991186287636:186287735:186287864:186287960:186289443:186289550186287864:186287960ENSG00000047410.9ENST00000367478.4,ENST00000467810.1
exon_skip_351011186292817:186293002:186294895:186294986:186295235:186295352186294895:186294986ENSG00000047410.9ENST00000367478.4
exon_skip_351041186294928:186294986:186295235:186295367:186296591:186296792186295235:186295367ENSG00000047410.9ENST00000367478.4
exon_skip_351061186296591:186296792:186300629:186300713:186301326:186301475186300629:186300713ENSG00000047410.9ENST00000367478.4
exon_skip_351081186303456:186303665:186304199:186304261:186304469:186304675186304199:186304261ENSG00000047410.9ENST00000367478.4
exon_skip_351091186307318:186307375:186308773:186308904:186310159:186310291186308773:186308904ENSG00000047410.9ENST00000367478.4,ENST00000481347.1
exon_skip_351101186310159:186310291:186310383:186310521:186312457:186312605186310383:186310521ENSG00000047410.9ENST00000367478.4
exon_skip_351131186321146:186321242:186322819:186322982:186324541:186324684186322819:186322982ENSG00000047410.9ENST00000367478.4,ENST00000491783.1
exon_skip_351151186321146:186321242:186322819:186323012:186324541:186324684186322819:186323012ENSG00000047410.9ENST00000474852.1
exon_skip_351181186332473:186332577:186337017:186337114:186340101:186340175186337017:186337114ENSG00000047410.9ENST00000474852.1,ENST00000367478.4

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

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Exon skipping events with PSIs in GTEx for TPR

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_350921186280783:186283158:186283760:186283856:186286613:186286732186283760:186283856ENSG00000047410.9ENST00000367478.4
exon_skip_350951186283760:186283856:186286613:186286732:186287578:186287735186286613:186286732ENSG00000047410.9ENST00000367478.4
exon_skip_350991186287636:186287735:186287864:186287960:186289443:186289550186287864:186287960ENSG00000047410.9ENST00000367478.4,ENST00000467810.1
exon_skip_351011186292817:186293002:186294895:186294986:186295235:186295352186294895:186294986ENSG00000047410.9ENST00000367478.4
exon_skip_351041186294928:186294986:186295235:186295367:186296591:186296792186295235:186295367ENSG00000047410.9ENST00000367478.4
exon_skip_351061186296591:186296792:186300629:186300713:186301326:186301475186300629:186300713ENSG00000047410.9ENST00000367478.4
exon_skip_351081186303456:186303665:186304199:186304261:186304469:186304675186304199:186304261ENSG00000047410.9ENST00000367478.4
exon_skip_351091186307318:186307375:186308773:186308904:186310159:186310291186308773:186308904ENSG00000047410.9ENST00000367478.4,ENST00000481347.1
exon_skip_351101186310159:186310291:186310383:186310521:186312457:186312605186310383:186310521ENSG00000047410.9ENST00000367478.4
exon_skip_351131186321146:186321242:186322819:186322982:186324541:186324684186322819:186322982ENSG00000047410.9ENST00000367478.4,ENST00000491783.1
exon_skip_351151186321146:186321242:186322819:186323012:186324541:186324684186322819:186323012ENSG00000047410.9ENST00000474852.1
exon_skip_351181186332473:186332577:186337017:186337114:186340101:186340175186337017:186337114ENSG00000047410.9ENST00000367478.4,ENST00000474852.1

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 TPR

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
ENST00000367478186286613186286732Frame-shift
ENST00000367478186294895186294986Frame-shift
ENST00000367478186304199186304261Frame-shift
ENST00000367478186308773186308904Frame-shift
ENST00000367478186322819186322982Frame-shift
ENST00000367478186337017186337114Frame-shift
ENST00000367478186283760186283856In-frame
ENST00000367478186287864186287960In-frame
ENST00000367478186295235186295367In-frame
ENST00000367478186300629186300713In-frame
ENST00000367478186310383186310521In-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
ENST00000367478186286613186286732Frame-shift
ENST00000367478186294895186294986Frame-shift
ENST00000367478186304199186304261Frame-shift
ENST00000367478186308773186308904Frame-shift
ENST00000367478186322819186322982Frame-shift
ENST00000367478186337017186337114Frame-shift
ENST00000367478186283760186283856In-frame
ENST00000367478186287864186287960In-frame
ENST00000367478186295235186295367In-frame
ENST00000367478186300629186300713In-frame
ENST00000367478186310383186310521In-frame

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

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
ENST00000367478972523631863103831863105214048418512501296
ENST00000367478972523631863006291863007135902598518681896
ENST00000367478972523631862952351862953676187631819632007
ENST00000367478972523631862878641862879606866696121892221
ENST00000367478972523631862837601862838567238733323132345

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
ENST00000367478972523631863103831863105214048418512501296
ENST00000367478972523631863006291863007135902598518681896
ENST00000367478972523631862952351862953676187631819632007
ENST00000367478972523631862878641862879606866696121892221
ENST00000367478972523631862837601862838567238733323132345

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
P12270125012967272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701250129622363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701250129612151630Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
P122701250129612181320RegionNote=Necessary for interaction with HSF1;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:17897941;Dbxref=PMID:17897941
P12270186818967272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701868189622363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701868189618931893Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:24275569;Dbxref=PMID:24275569
P12270196320077272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701963200722363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701963200719711978Compositional biasNote=Poly-Asp
P122701963200719521965Sequence conflictNote=Missing;Ontology_term=ECO:0000305;evidence=ECO:0000305
P12270218922217272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122702189222122363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P12270231323457272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122702313234522363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122702313234523432343Modified residueNote=Asymmetric dimethylarginine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:F6ZDS4
P122702313234523452345Modified residueNote=Asymmetric dimethylarginine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:F6ZDS4


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
P12270125012967272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701250129622363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701250129612151630Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
P122701250129612181320RegionNote=Necessary for interaction with HSF1;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:17897941;Dbxref=PMID:17897941
P12270186818967272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701868189622363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701868189618931893Modified residueNote=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244|PubMed:24275569;Dbxref=PMID:24275569
P12270196320077272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122701963200722363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122701963200719711978Compositional biasNote=Poly-Asp
P122701963200719521965Sequence conflictNote=Missing;Ontology_term=ECO:0000305;evidence=ECO:0000305
P12270218922217272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122702189222122363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P12270231323457272363Alternative sequenceID=VSP_057407;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:1549355;Dbxref=PMID:1549355
P122702313234522363ChainID=PRO_0000204920;Note=Nucleoprotein TPR
P122702313234523432343Modified residueNote=Asymmetric dimethylarginine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:F6ZDS4
P122702313234523452345Modified residueNote=Asymmetric dimethylarginine;Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:F6ZDS4


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SNVs in the skipped exons for TPR

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_35099
186287865186287960186287943186287943Frame_Shift_DelT-p.T2196fs
LIHCTCGA-DD-A3A0-01exon_skip_35101
186294896186294986186294963186294963Frame_Shift_DelA-p.G2015fs
BLCATCGA-ZF-A9R0-01exon_skip_35104
186295236186295367186295316186295316Frame_Shift_DelT-p.M1981fs
LIHCTCGA-G3-A3CJ-01186304200186304261186304228186304228Frame_Shift_DelT-p.T1650fs
BLCATCGA-XF-A9T6-01exon_skip_35118
186337018186337114186337095186337105Frame_Shift_DelTTTGTTCTTGT-p.TRTK114fs
BLCATCGA-GC-A3OO-01exon_skip_35092
186283761186283856186283842186283842Nonsense_MutationGAp.Q2319*
STADTCGA-D7-A4YV-01exon_skip_35110
186310384186310521186310500186310500Nonsense_MutationGAp.Q1258*
STADTCGA-D7-A4YV-01exon_skip_35110
186310384186310521186310500186310500Nonsense_MutationGAp.Q1258X
UCECTCGA-AP-A0LM-01exon_skip_35113
186322820186322982186322945186322945Nonsense_MutationGAp.R737*
UCECTCGA-AP-A0LM-01exon_skip_35115
186322820186323012186322945186322945Nonsense_MutationGAp.R737*
UCECTCGA-BS-A0UV-01exon_skip_35113
186322820186322982186322945186322945Nonsense_MutationGAp.R737*
UCECTCGA-BS-A0UV-01exon_skip_35115
186322820186323012186322945186322945Nonsense_MutationGAp.R737*
READTCGA-F5-6814-01exon_skip_35118
186337018186337114186337090186337090Nonsense_MutationCAp.E119X
LUSCTCGA-18-3409-01exon_skip_35106
186300630186300713186300714186300714Splice_SiteCTp.E1869_splice

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
SW48_LARGE_INTESTINE186337018186337114186337050186337053Frame_Shift_DelTCAT-p.NE131fs
LOVO_LARGE_INTESTINE186283761186283856186283802186283802Missense_MutationAGp.L2332S
A704_KIDNEY186283761186283856186283803186283803Missense_MutationACp.L2332V
GP2D_LARGE_INTESTINE186283761186283856186283854186283854Missense_MutationTCp.T2315A
REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE186283761186283856186283854186283854Missense_MutationTCp.T2315A
HEC108_ENDOMETRIUM186287865186287960186287870186287870Missense_MutationGAp.A2220V
BICR18_UPPER_AERODIGESTIVE_TRACT186294896186294986186294921186294921Missense_MutationGCp.H2029Q
BICR18_UPPER_AERODIGESTIVE_TRACT186294896186294986186294929186294929Missense_MutationCTp.G2027S
BICR18_UPPER_AERODIGESTIVE_TRACT186294896186294986186294934186294934Missense_MutationCGp.G2025A
MHHCALL4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE186294896186294986186294935186294935Missense_MutationCAp.G2025C
MZ7MEL_SKIN186294896186294986186294964186294964Missense_MutationCTp.G2015D
ISHIKAWAHERAKLIO02ER_ENDOMETRIUM186295236186295367186295259186295259Missense_MutationCAp.G2000C
DMS153_LUNG186295236186295367186295262186295262Missense_MutationCAp.D1999Y
LNCAPCLONEFGC_PROSTATE186295236186295367186295294186295294Missense_MutationCAp.S1988I
AN3CA_ENDOMETRIUM186295236186295367186295322186295322Missense_MutationTGp.T1979P
NCIH1838_LUNG186295236186295367186295330186295330Missense_MutationTCp.E1976G
BT483_BREAST186295236186295367186295337186295337Missense_MutationCTp.D1974N
HEC108_ENDOMETRIUM186300630186300713186300646186300646Missense_MutationTCp.Q1891R
HELA_CERVIX186310384186310521186310393186310393Missense_MutationCTp.M1293I
HCC2998_LARGE_INTESTINE186310384186310521186310407186310407Missense_MutationCTp.D1289N
NCIH2052_PLEURA186310384186310521186310431186310431Missense_MutationCTp.E1281K
COLO775_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE186310384186310521186310480186310480Missense_MutationCAp.K1264N
NCIH2023_LUNG186310384186310521186310504186310504Missense_MutationCAp.M1256I
EFO21_OVARY186322820186322982186322853186322853Missense_MutationCGp.L767F
EFO21_OVARY186322820186323012186322853186322853Missense_MutationCGp.L767F
MFE319_ENDOMETRIUM186322820186322982186322906186322906Missense_MutationTCp.T750A
MFE319_ENDOMETRIUM186322820186323012186322906186322906Missense_MutationTCp.T750A

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

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 TPR


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


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RelatedDrugs for TPR

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 TPR

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
TPRC0040136Thyroid Neoplasm1CTD_human