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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 TSPAN14

check button Gene summary
Gene informationGene symbol

TSPAN14

Gene ID

81619

Gene nametetraspanin 14
SynonymsDC-TM4F2|TM4SF14
Cytomap

10q23.1

Type of geneprotein-coding
Descriptiontetraspanin-14tetraspanin similar to TM4SF9transmembrane 4 superfamily member 14tspan-14
Modification date20180523
UniProtAcc

Q8NG11

ContextPubMed: TSPAN14 [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 TSPAN14 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 TSPAN14

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 TSPAN14

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_433351082214110:82214127:82222843:82222883:82228302:8222844382222843:82222883ENSG00000108219.10ENST00000372158.1
exon_skip_433481082214110:82214127:82248972:82249070:82264483:8226453382248972:82249070ENSG00000108219.10ENST00000469149.1,ENST00000372157.2,ENST00000341863.6
exon_skip_433491082214110:82214127:82248972:82249070:82266983:8226705282248972:82249070ENSG00000108219.10ENST00000372164.3
exon_skip_433721082222843:82222883:82226196:82226294:82228302:8222844382226196:82226294ENSG00000108219.10ENST00000372156.1
exon_skip_433751082222843:82222883:82228302:82228443:82248972:8224907082228302:82228443ENSG00000108219.10ENST00000372158.1
exon_skip_433821082228337:82228443:82248972:82249070:82264483:8226453482248972:82249070ENSG00000108219.10ENST00000372158.1,ENST00000372156.1
exon_skip_433951082248972:82249070:82264483:82264534:82266954:8226713082264483:82264534ENSG00000108219.10ENST00000372157.2
exon_skip_433961082248972:82249070:82264483:82264534:82266983:8226705282264483:82264534ENSG00000108219.10ENST00000469149.1,ENST00000372158.1,ENST00000429989.3,ENST00000341863.6,ENST00000372156.1
exon_skip_434031082248972:82249070:82266983:82267130:82269056:8226922782266983:82267130ENSG00000108219.10ENST00000372164.3
exon_skip_434061082264483:82264534:82266954:82267130:82269056:8226922782266954:82267130ENSG00000108219.10ENST00000372157.2
exon_skip_434101082264483:82264534:82266983:82267130:82269056:8226922782266983:82267130ENSG00000108219.10ENST00000469149.1,ENST00000372158.1,ENST00000429989.3,ENST00000372156.1
exon_skip_434111082264483:82264534:82266983:82267130:82271899:8227202582266983:82267130ENSG00000108219.10ENST00000341863.6
exon_skip_434141082266983:82267130:82269056:82269227:82271899:8227202582269056:82269227ENSG00000108219.10ENST00000372157.2,ENST00000372158.1,ENST00000429989.3,ENST00000372164.3,ENST00000372156.1
exon_skip_434151082271899:82272025:82273774:82273819:82275959:8227607982273774:82273819ENSG00000108219.10ENST00000372157.2,ENST00000481124.1,ENST00000372158.1,ENST00000429989.3,ENST00000372164.3,ENST00000341863.6,ENST00000372156.1
exon_skip_434161082273774:82273819:82275959:82276079:82277660:8227767882275959:82276079ENSG00000108219.10ENST00000372157.2,ENST00000481124.1,ENST00000372158.1,ENST00000429989.3,ENST00000372164.3,ENST00000341863.6,ENST00000372156.1

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

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Exon skipping events with PSIs in GTEx for TSPAN14

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_433351082214110:82214127:82222843:82222883:82228302:8222844382222843:82222883ENSG00000108219.10ENST00000372158.1
exon_skip_433481082214110:82214127:82248972:82249070:82264483:8226453382248972:82249070ENSG00000108219.10ENST00000372157.2,ENST00000469149.1,ENST00000341863.6
exon_skip_433491082214110:82214127:82248972:82249070:82266983:8226705282248972:82249070ENSG00000108219.10ENST00000372164.3
exon_skip_433721082222843:82222883:82226196:82226294:82228302:8222844382226196:82226294ENSG00000108219.10ENST00000372156.1
exon_skip_433751082222843:82222883:82228302:82228443:82248972:8224907082228302:82228443ENSG00000108219.10ENST00000372158.1
exon_skip_433821082228337:82228443:82248972:82249070:82264483:8226453482248972:82249070ENSG00000108219.10ENST00000372158.1,ENST00000372156.1
exon_skip_433951082248972:82249070:82264483:82264534:82266954:8226713082264483:82264534ENSG00000108219.10ENST00000372157.2
exon_skip_433961082248972:82249070:82264483:82264534:82266983:8226705282264483:82264534ENSG00000108219.10ENST00000429989.3,ENST00000469149.1,ENST00000372158.1,ENST00000341863.6,ENST00000372156.1
exon_skip_434031082248972:82249070:82266983:82267130:82269056:8226922782266983:82267130ENSG00000108219.10ENST00000372164.3
exon_skip_434061082264483:82264534:82266954:82267130:82269056:8226922782266954:82267130ENSG00000108219.10ENST00000372157.2
exon_skip_434101082264483:82264534:82266983:82267130:82269056:8226922782266983:82267130ENSG00000108219.10ENST00000429989.3,ENST00000469149.1,ENST00000372158.1,ENST00000372156.1
exon_skip_434111082264483:82264534:82266983:82267130:82271899:8227202582266983:82267130ENSG00000108219.10ENST00000341863.6
exon_skip_434141082266983:82267130:82269056:82269227:82271899:8227202582269056:82269227ENSG00000108219.10ENST00000429989.3,ENST00000372157.2,ENST00000372164.3,ENST00000372158.1,ENST00000372156.1
exon_skip_434151082271899:82272025:82273774:82273819:82275959:8227607982273774:82273819ENSG00000108219.10ENST00000429989.3,ENST00000481124.1,ENST00000372157.2,ENST00000372164.3,ENST00000372158.1,ENST00000341863.6,ENST00000372156.1
exon_skip_434161082273774:82273819:82275959:82276079:82277660:8227767882275959:82276079ENSG00000108219.10ENST00000429989.3,ENST00000481124.1,ENST00000372157.2,ENST00000372164.3,ENST00000372158.1,ENST00000341863.6,ENST00000372156.1

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 TSPAN14

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
ENST0000037215682248972822490705CDS-5UTR
ENST0000037215882248972822490705CDS-5UTR
ENST0000037215882222843822228835UTR-5UTR
ENST0000037215682226196822262945UTR-5UTR
ENST0000037215882228302822284435UTR-5UTR
ENST000003721568226448382264534In-frame
ENST000003721588226448382264534In-frame
ENST000004299898226448382264534In-frame
ENST000003721568226698382267130In-frame
ENST000003721588226698382267130In-frame
ENST000004299898226698382267130In-frame
ENST000003721568226905682269227In-frame
ENST000003721588226905682269227In-frame
ENST000004299898226905682269227In-frame
ENST000003721568227377482273819In-frame
ENST000003721588227377482273819In-frame
ENST000004299898227377482273819In-frame
ENST000003721568227595982276079In-frame
ENST000003721588227595982276079In-frame
ENST000004299898227595982276079In-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
ENST0000037215682248972822490705CDS-5UTR
ENST0000037215882248972822490705CDS-5UTR
ENST0000037215882222843822228835UTR-5UTR
ENST0000037215682226196822262945UTR-5UTR
ENST0000037215882228302822284435UTR-5UTR
ENST000003721568226448382264534In-frame
ENST000003721588226448382264534In-frame
ENST000004299898226448382264534In-frame
ENST000003721568226698382267130In-frame
ENST000003721588226698382267130In-frame
ENST000004299898226698382267130In-frame
ENST000003721568226905682269227In-frame
ENST000003721588226905682269227In-frame
ENST000004299898226905682269227In-frame
ENST000003721568227377482273819In-frame
ENST000003721588227377482273819In-frame
ENST000004299898227377482273819In-frame
ENST000003721568227595982276079In-frame
ENST000003721588227595982276079In-frame
ENST000004299898227595982276079In-frame

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Infer the effects of exon skipping event on protein functional features for TSPAN14

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
ENST00000372156139727082264483822645345846342744
ENST00000372158111227082264483822645342993492744
ENST000004299891620027082264483822645343053552744
ENST00000372156139727082266983822671306357814493
ENST00000372158111227082266983822671303504964493
ENST000004299891620027082266983822671303565024493
ENST000003721561397270822690568226922778295293150
ENST000003721581112270822690568226922749766793150
ENST0000042998916200270822690568226922750367393150
ENST000003721561397270822737748227381910791123192207
ENST0000037215811122708227377482273819794838192207
ENST00000429989162002708227377482273819800844192207
ENST000003721561397270822759598227607911241243207247
ENST0000037215811122708227595982276079839958207247
ENST00000429989162002708227595982276079845964207247

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
ENST00000372156139727082264483822645345846342744
ENST00000372158111227082264483822645342993492744
ENST000004299891620027082264483822645343053552744
ENST00000372156139727082266983822671306357814493
ENST00000372158111227082266983822671303504964493
ENST000004299891620027082266983822671303565024493
ENST000003721561397270822690568226922778295293150
ENST000003721581112270822690568226922749766793150
ENST0000042998916200270822690568226922750367393150
ENST000003721561397270822737748227381910791123192207
ENST0000037215811122708227377482273819794838192207
ENST00000429989162002708227377482273819800844192207
ENST000003721561397270822759598227607911241243207247
ENST0000037215811122708227595982276079839958207247
ENST00000429989162002708227595982276079845964207247

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
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255


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
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11274428150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127442844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127441270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127443961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1127441838TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11449328150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144932844Alternative sequenceID=VSP_011878;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:15489334;Dbxref=PMID:15489334
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144931270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144933961Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144938392Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG1144936282TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11449393113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG119315028150Alternative sequenceID=VSP_043194;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:14702039;Dbxref=PMID:14702039
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11931501270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150143143Sequence conflictNote=L->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG1193150114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG119315093113TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG111922071270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11192207114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG112072471270ChainID=PRO_0000219261;Note=Tetraspanin-14
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232RegionNote=Necessary and sufficient for interaction with ADAM10;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26668317;Dbxref=PMID:26668317
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247114232Topological domainNote=Extracellular;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q8NG11207247233253TransmembraneNote=Helical;Ontology_term=ECO:0000255;evidence=ECO:0000255


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SNVs in the skipped exons for TSPAN14

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
HNSCTCGA-CV-7097-01exon_skip_43348
exon_skip_43349
exon_skip_43382
82248973822490708224906982249069Frame_Shift_DelG-p.W27fs
LIHCTCGA-DD-A1EG-01exon_skip_43410
exon_skip_43411
exon_skip_43406
exon_skip_43403
82266955822671308226703182267031Frame_Shift_DelC-p.D60fs
LIHCTCGA-DD-A1EG-01exon_skip_43410
exon_skip_43411
exon_skip_43406
exon_skip_43403
82266984822671308226703182267031Frame_Shift_DelC-p.D60fs
LIHCTCGA-G3-A3CJ-01exon_skip_43410
exon_skip_43411
exon_skip_43406
exon_skip_43403
82266955822671308226707682267076Frame_Shift_DelG-p.L75fs
LIHCTCGA-G3-A3CJ-01exon_skip_43410
exon_skip_43411
exon_skip_43406
exon_skip_43403
82266984822671308226707682267076Frame_Shift_DelG-p.L75fs
LIHCTCGA-DD-A1EG-01exon_skip_43414
82269057822692278226908182269081Frame_Shift_DelT-p.F103fs
LIHCTCGA-DD-A1EG-01exon_skip_43414
82269057822692278226919982269199Frame_Shift_DelA-p.Q141fs

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
MN60_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE82264484822645348226451182264511Missense_MutationGAp.G37R
RERFLCAD1_LUNG82264484822645348226451982264519Missense_MutationGTp.W39C
NCIH2172_LUNG82266984822671308226701782267017Missense_MutationATp.M56L
NCIH2172_LUNG82266955822671308226701782267017Missense_MutationATp.M56L
BE2M17_AUTONOMIC_GANGLIA82266984822671308226706882267068Missense_MutationTCp.F73L
BE2M17_AUTONOMIC_GANGLIA82266955822671308226706882267068Missense_MutationTCp.F73L
SKNBE2_AUTONOMIC_GANGLIA82266984822671308226706882267068Missense_MutationTCp.F73L
SKNBE2_AUTONOMIC_GANGLIA82266955822671308226706882267068Missense_MutationTCp.F73L
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE82266984822671308226708082267080Missense_MutationTCp.F77L
DND41_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE82266955822671308226708082267080Missense_MutationTCp.F77L
NCIH661_LUNG82266984822671308226709282267092Missense_MutationGCp.V81L
NCIH661_LUNG82266955822671308226709282267092Missense_MutationGCp.V81L
JHUEM1_ENDOMETRIUM82269057822692278226907882269078Missense_MutationAGp.I101V
DG75_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE82269057822692278226910582269105Missense_MutationGAp.V110M
HEC265_ENDOMETRIUM82269057822692278226911182269111Missense_MutationGAp.A112T
LS411N_LARGE_INTESTINE82275960822760798227602082276020Missense_MutationTCp.W228R
HCT15_LARGE_INTESTINE82275960822760798227602282276022Nonsense_MutationGAp.W228*
BICR18_UPPER_AERODIGESTIVE_TRACT82264484822645348226448482264484Splice_SiteTCp.L28L

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for TSPAN14

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 TSPAN14


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for TSPAN14


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RelatedDrugs for TSPAN14

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 TSPAN14

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