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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 PKN3

check button Gene summary
Gene informationGene symbol

PKN3

Gene ID

29941

Gene nameprotein kinase N3
SynonymsUTDP4-1
Cytomap

9q34.11

Type of geneprotein-coding
Descriptionserine/threonine-protein kinase N3protein kinase PKN-betaprotein-kinase C-related kinase 3
Modification date20180523
UniProtAcc

Q6P5Z2

ContextPubMed: PKN3 [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
PKN3

GO:0010631

epithelial cell migration

21754995


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Exon skipping events across known transcript of Ensembl for PKN3 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 PKN3

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 PKN3

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_4998219131475395:131475477:131475556:131475666:131475777:131475921131475556:131475666ENSG00000160447.6ENST00000291906.4,ENST00000483521.1
exon_skip_4998249131475777:131475921:131476324:131476400:131476475:131476644131476324:131476400ENSG00000160447.6ENST00000291906.4
exon_skip_4998259131476884:131476943:131477076:131477144:131477450:131477514131477076:131477144ENSG00000160447.6ENST00000485301.1,ENST00000291906.4
exon_skip_4998269131477450:131477514:131477647:131477739:131479025:131479202131477647:131477739ENSG00000160447.6ENST00000291906.4
exon_skip_4998279131477647:131477739:131479025:131479202:131480603:131480666131479025:131479202ENSG00000160447.6ENST00000291906.4
exon_skip_4998289131479025:131479202:131480603:131480666:131480827:131480904131480603:131480666ENSG00000160447.6ENST00000485301.1,ENST00000291906.4
exon_skip_4998329131480603:131480666:131480827:131480904:131481964:131482107131480827:131480904ENSG00000160447.6ENST00000485301.1,ENST00000291906.4

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

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Exon skipping events with PSIs in GTEx for PKN3

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_4998219131475395:131475477:131475556:131475666:131475777:131475921131475556:131475666ENSG00000160447.6ENST00000291906.4,ENST00000483521.1
exon_skip_4998249131475777:131475921:131476324:131476400:131476475:131476644131476324:131476400ENSG00000160447.6ENST00000291906.4
exon_skip_4998259131476884:131476943:131477076:131477144:131477450:131477514131477076:131477144ENSG00000160447.6ENST00000291906.4,ENST00000485301.1
exon_skip_4998269131477450:131477514:131477647:131477739:131479025:131479202131477647:131477739ENSG00000160447.6ENST00000291906.4
exon_skip_4998279131477647:131477739:131479025:131479202:131480603:131480666131479025:131479202ENSG00000160447.6ENST00000291906.4
exon_skip_4998289131479025:131479202:131480603:131480666:131480827:131480904131480603:131480666ENSG00000160447.6ENST00000291906.4,ENST00000485301.1
exon_skip_4998329131480603:131480666:131480827:131480904:131481964:131482107131480827:131480904ENSG00000160447.6ENST00000291906.4,ENST00000485301.1

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 PKN3

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
ENST00000291906131475556131475666Frame-shift
ENST00000291906131476324131476400Frame-shift
ENST00000291906131477076131477144Frame-shift
ENST00000291906131477647131477739Frame-shift
ENST00000291906131480827131480904Frame-shift
ENST00000291906131479025131479202In-frame
ENST00000291906131480603131480666In-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
ENST00000291906131475556131475666Frame-shift
ENST00000291906131476324131476400Frame-shift
ENST00000291906131477076131477144Frame-shift
ENST00000291906131477647131477739Frame-shift
ENST00000291906131480827131480904Frame-shift
ENST00000291906131479025131479202In-frame
ENST00000291906131480603131480666In-frame

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Infer the effects of exon skipping event on protein functional features for PKN3

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
ENST00000291906339288913147902513147920222022378603661
ENST00000291906339288913148060313148066623792441662682

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
ENST00000291906339288913147902513147920222022378603661
ENST00000291906339288913148060313148066623792441662682

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
Q6P5Z26036611889ChainID=PRO_0000055725;Note=Serine/threonine-protein kinase N3
Q6P5Z2603661559818DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
Q6P5Z2603661627627Sequence conflictNote=A->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q6P5Z2603661636636Sequence conflictNote=C->R;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q6P5Z26626821889ChainID=PRO_0000055725;Note=Serine/threonine-protein kinase N3
Q6P5Z2662682559818DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159


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
Q6P5Z26036611889ChainID=PRO_0000055725;Note=Serine/threonine-protein kinase N3
Q6P5Z2603661559818DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
Q6P5Z2603661627627Sequence conflictNote=A->V;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q6P5Z2603661636636Sequence conflictNote=C->R;Ontology_term=ECO:0000305;evidence=ECO:0000305
Q6P5Z26626821889ChainID=PRO_0000055725;Note=Serine/threonine-protein kinase N3
Q6P5Z2662682559818DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159


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SNVs in the skipped exons for PKN3

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
UCECTCGA-EY-A212-01exon_skip_499828
131480604131480666131480644131480644Frame_Shift_DelC-p.H676fs
LIHCTCGA-DD-A3A0-01exon_skip_499832
131480828131480904131480860131480860Frame_Shift_DelC-p.A694fs
KIRPTCGA-5P-A9K6-01exon_skip_499825
131477077131477144131477092131477093Frame_Shift_Ins-ATp.H534fs
UCECTCGA-FI-A2EX-01exon_skip_499828
131480604131480666131480610131480610Nonsense_MutationCGp.Y664*
KIRCTCGA-B0-4811-01exon_skip_499832
131480828131480904131480826131480826Splice_SiteAC.

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
PCI15A_UPPER_AERODIGESTIVE_TRACT131477648131477739131477734131477737Frame_Shift_DelAGAG-p.IE601fs
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE131480604131480666131480648131480650In_Frame_DelAGA-p.K679del
SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE131475557131475666131475590131475590Missense_MutationGAp.R339H
SUPT1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE131476325131476400131476355131476355Missense_MutationCTp.R423W
SUPHD1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE131476325131476400131476380131476380Missense_MutationGAp.R431H
OUMS23_LARGE_INTESTINE131476325131476400131476380131476380Missense_MutationGAp.R431H
SW684_SOFT_TISSUE131477077131477144131477089131477089Missense_MutationCTp.P533S
SW48_LARGE_INTESTINE131477077131477144131477137131477137Missense_MutationCTp.P549S
EN_ENDOMETRIUM131479026131479202131479037131479037Missense_MutationAGp.E607G
NCIH2172_LUNG131479026131479202131479076131479076Missense_MutationCAp.P620H
REH_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE131479026131479202131479144131479144Missense_MutationCTp.P643S
MKN7_STOMACH131480604131480666131480609131480609Missense_MutationAGp.Y664C
ASH3_THYROID131480604131480666131480609131480609Missense_MutationAGp.Y664C
TE15_OESOPHAGUS131480604131480666131480609131480609Missense_MutationAGp.Y664C
CORL303_LUNG131480604131480666131480658131480658Missense_MutationCGp.I680M
MFE296_ENDOMETRIUM131480828131480904131480847131480847Missense_MutationCTp.L690F
NCIH2141_LUNG131480828131480904131480860131480860Missense_MutationCAp.A694D
TE9_OESOPHAGUS131480828131480904131480889131480889Missense_MutationGAp.G704R
SNUC5_LARGE_INTESTINE131477077131477144131477078131477078Splice_SiteGAp.R529H
CCK81_LARGE_INTESTINE131479026131479202131479027131479027Splice_SiteCTp.L604L

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for PKN3

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 PKN3


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for PKN3


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RelatedDrugs for PKN3

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 PKN3

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