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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 RPSMAP, MSBB, and Mayo

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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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3'-UTR located exon skipping events lost miRNA binding sites

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SNVs in the skipped exons with depth of coverage

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AD stage-associated exon skipping events

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Correlation with RNA binding proteins (RBPs)

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Related drugs with this gene

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Related diseases with this gene

Gene summary for PRKD2

check button Gene summary
Gene informationGene symbol

PRKD2

Gene ID

25865

Gene nameprotein kinase D2
SynonymsHSPC187|PKD2|nPKC-D2
Cytomap

19q13.32

Type of geneprotein-coding
Descriptionserine/threonine-protein kinase D2
Modification date20200329
UniProtAcc

A0JLT6,

M0QXC6,

M0QZ82,

M0QZC2,

M0R012,

M0R2Z8,

M0R346,

Context

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
PRKD2

GO:0006468

protein phosphorylation

22228765

PRKD2

GO:0018105

peptidyl-serine phosphorylation

18440775

PRKD2

GO:0045944

positive regulation of transcription by RNA polymerase II

17077180

PRKD2

GO:0046777

protein autophosphorylation

17077180

PRKD2

GO:0050852

T cell receptor signaling pathway

17077180


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Gene structures and expression levels for PRKD2

check buttonSkipped exons in the ROSMAP, MSBB, and Mayo 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

ENSG00000105287
check button Differentially expressed gene analysis across multiple brain tissues between AD and control.
Tissue typeDEG directionBase mean exp.log2FC(AD/control)P-valueAdj. p-value

check button Differentially expressed isoform analysis across multiple brain tissues between AD and control.
gencode gene structure
Tissue typeDEG directionENSTTranscript info.Base mean exp.log2FC(AD/control)P-valueAdjc. p-value
PGUPENST00000291281.8PRKD2-201:protein_coding:PRKD21.907686e+011.494065e+001.405606e-043.526166e-03
CBDOWNENST00000602155.5PRKD2-217:retained_intron:PRKD22.217501e+01-8.970672e-012.809276e-031.222066e-02

check button Landscape of isoform expressions across multiple brain tissues between AD and control.
gencode gene structure

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Exon skipping events with PSIs in ROSMAP, MSBB, and Mayo for PRKD2

check button Landscape of individual exon skipping event across AD tissues and controls (PSI heatmap).
boxplot

check button All exon skipping events in AD cohorts.
Exon skip IDchrExons involved in exon skippingSkipped exon
exon_skip_110416chr1946675033:46675118:46678396:46678663:46681650:4668174846678396:46678663
exon_skip_181019chr1946700799:46700952:46701035:46701112:46704169:4670439146701035:46701112
exon_skip_187606chr1946710907:46711038:46713863:46714001:46716131:4671624446713863:46714001
exon_skip_260419chr1946681683:46681748:46685425:46685521:46689537:4668969846685425:46685521
exon_skip_281714chr1946710907:46711038:46713863:46714001:46716131:4671622046713863:46714001
exon_skip_287895chr1946690600:46690706:46691735:46691807:46691933:4669198546691735:46691807
exon_skip_68938chr1946675033:46675118:46678366:46678663:46681650:4668174846678366:46678663

check button Differentially expressed PSI values of individual exon skipping events in multiple brain tissues between AD and control.
Exon skipping informationTissue typeAvg(PSIs) in ADAvg(PSIs) in controlDifference (PSI)Adj. p-value


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Open reading frame (ORF) annotation in the exon skipping event for PRKD2

check button Open reading frame (ORF) of individual exon skipping events in ROSMAP based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002912814667839646678663Frame-shift
ENST000004338674667839646678663Frame-shift
ENST000002912814669173546691807Frame-shift
ENST000004338674669173546691807Frame-shift
ENST000002912814671386346714001Frame-shift
ENST000004338674671386346714001Frame-shift
ENST000002912814670103546701112In-frame
ENST000004338674670103546701112In-frame

check button Open reading frame (ORF) of individual exon skipping events in MSBB based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF

check button Open reading frame (ORF) of individual exon skipping events in Mayo based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002912814667839646678663Frame-shift
ENST000004338674667839646678663Frame-shift
ENST000002912814671386346714001Frame-shift
ENST000004338674671386346714001Frame-shift
ENST000002912814670103546701112In-frame
ENST000004338674670103546701112In-frame

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Infer the effects of exon skipping event on protein functional features for PRKD2

p-ENSG00000105287_img4.png
boxplot

check button Loci of skipped exons in ROSMAP across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST000002912813087878467010354670111211161192296322
ENST000004338673338878467010354670111213681444296322

check button Loci of skipped exons in MSBB across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end

check button Loci of skipped exons in Mayo across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST000002912813087878467010354670111211161192296322
ENST000004338673338878467010354670111213681444296322

check button Lost protein functional features of individual exon skipping events in ROSMAP.
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
Q9BZL62963221878ChainID=PRO_0000055716;Note=Serine/threonine-protein kinase D2
Q9BZL62963221878ChainID=PRO_0000055716;Note=Serine/threonine-protein kinase D2
Q9BZL6296322264314Zinc fingerNote=Phorbol-ester/DAG-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00226
Q9BZL6296322264314Zinc fingerNote=Phorbol-ester/DAG-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00226

check button Lost protein functional features of individual exon skipping events in MSBB.
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

check button Lost protein functional features of individual exon skipping events in Mayo.
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
Q9BZL62963221878ChainID=PRO_0000055716;Note=Serine/threonine-protein kinase D2
Q9BZL62963221878ChainID=PRO_0000055716;Note=Serine/threonine-protein kinase D2
Q9BZL6296322264314Zinc fingerNote=Phorbol-ester/DAG-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00226
Q9BZL6296322264314Zinc fingerNote=Phorbol-ester/DAG-type 2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00226


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3'-UTR located exon skipping events that lost miRNA binding sites in PRKD2

check button 3'-UTR exon skipping evnets lost miRNA binding.
Tissue typeENSTExon skip startExon skip endmicroRNABinding site by TargetScanBinding type by TargetScanBdinding site by miRandaScore of miRandaEnergy by miRanda

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SNVs in the skipped exons for PRKD2

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

check button - Depth of Coverage in the skipped exon of the mutated samples.

check button - Sashimi plot in the skipped exon of the mutated samples.

check button - Non-synonymous mutations located in the skipped exons.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange

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AD stage-associated exon skippint events for PRKD2

check button Associated exon skipping events with Braak staging or Clinical Dementia Rating (CDR).
AD stage infoCohortTissueSE idCoefficient P-valueChromosomeStrandE1 startE1 endSkipped startSkipped endE2 startE2 end

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for PRKD2

check button sQTL information located at the skipped exons.
Tissue typeExon skip IDSNP idLocationP-valueFDR
TCexon_skip_260419rs3027957chr19:467842508.108568e-051.382573e-02
HCCexon_skip_260419rs4802322chr19:467397352.128234e-041.703576e-02
HCCexon_skip_260419rs11668987chr19:467245642.863386e-042.171122e-02
HCCexon_skip_260419rs314661chr19:466692168.107892e-044.954529e-02
PCCexon_skip_260419rs4802322chr19:467397355.752246e-093.538823e-06
PCCexon_skip_260419rs11668987chr19:467245642.741828e-071.132007e-04
PCCexon_skip_260419rs3027957chr19:467842503.233930e-069.618407e-04
DLPFCexon_skip_260419rs11668987chr19:467245641.009160e-071.885606e-05
DLPFCexon_skip_260419rs4802322chr19:467397351.337431e-072.417840e-05
DLPFCexon_skip_260419rs2871987chr19:466722712.524588e-052.546587e-03
DLPFCexon_skip_260419rs314661chr19:466692165.267532e-054.850631e-03
DLPFCexon_skip_260419rs3027957chr19:467842505.560314e-055.075473e-03
DLPFCexon_skip_260419rs12461093chr19:466826627.197512e-056.364712e-03
DLPFCexon_skip_260419rs314662chr19:466673871.789315e-041.394815e-02

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Correlation with RNA binding proteins (RBPs) for PRKD2

check button Correlated RBP and related information.
Tissue typeRBP nameExon skip IDCorrelation coeifficientP-value

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RelatedDrugs for PRKD2

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
UniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for PRKD2

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