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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:CSNK1D-VCP

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CSNK1D-VCP
FusionPDB ID: 19827
FusionGDB2.0 ID: 19827
HgeneTgene
Gene symbol

CSNK1D

VCP

Gene ID

1453

7415

Gene namecasein kinase 1 deltavalosin containing protein
SynonymsASPS|CKI-delta|CKId|CKIdelta|FASPS2|HCKIDCDC48|TERA|p97
Cytomap

17q25.3

9p13.3

Type of geneprotein-codingprotein-coding
Descriptioncasein kinase I isoform deltacasein kinase Itau-protein kinase CSNK1Dtransitional endoplasmic reticulum ATPase15S Mg(2+)-ATPase p97 subunitTER ATPase
Modification date2020031320200327
UniProtAcc

P48730

.
Ensembl transtripts involved in fusion geneENST idsENST00000578904, ENST00000392334, 
ENST00000314028, ENST00000398519, 
ENST00000358901, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score17 X 16 X 13=353611 X 13 X 3=429
# samples 2414
** MAII scorelog2(24/3536*10)=-3.88101196378291
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/429*10)=-1.61555082055458
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CSNK1D [Title/Abstract] AND VCP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CSNK1D(80213304)-VCP(35059798), # samples:1
Anticipated loss of major functional domain due to fusion event.CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CSNK1D-VCP seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneCSNK1D

GO:0006468

protein phosphorylation

16618118

HgeneCSNK1D

GO:0018105

peptidyl-serine phosphorylation

25500533

HgeneCSNK1D

GO:0051225

spindle assembly

10826492

TgeneVCP

GO:0006302

double-strand break repair

10855792|22120668

TgeneVCP

GO:0006974

cellular response to DNA damage stimulus

16140914|22120668|23042605

TgeneVCP

GO:0016567

protein ubiquitination

22120668

TgeneVCP

GO:0030433

ubiquitin-dependent ERAD pathway

17872946

TgeneVCP

GO:0030970

retrograde protein transport, ER to cytosol

15215856

TgeneVCP

GO:0031334

positive regulation of protein complex assembly

18775313

TgeneVCP

GO:0032436

positive regulation of proteasomal ubiquitin-dependent protein catabolic process

9452483

TgeneVCP

GO:0036503

ERAD pathway

25088257

TgeneVCP

GO:0045732

positive regulation of protein catabolic process

11483959|18775313

TgeneVCP

GO:0090263

positive regulation of canonical Wnt signaling pathway

28689657

TgeneVCP

GO:1903006

positive regulation of protein K63-linked deubiquitination

22970133

TgeneVCP

GO:1903007

positive regulation of Lys63-specific deubiquitinase activity

22970133


check buttonFusion gene breakpoints across CSNK1D (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across VCP (3'-gene)
* 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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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-D7-A6EZCSNK1Dchr17

80213304

-VCPchr9

35059798

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000398519CSNK1Dchr1780213304-ENST00000358901VCPchr935059798-2162383471108353
ENST00000314028CSNK1Dchr1780213304-ENST00000358901VCPchr935059798-2465686111411466

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000398519ENST00000358901CSNK1Dchr1780213304-VCPchr935059798-0.0019675840.9980324
ENST00000314028ENST00000358901CSNK1Dchr1780213304-VCPchr935059798-0.0022952090.9977048

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>19827_19827_1_CSNK1D-VCP_CSNK1D_chr17_80213304_ENST00000314028_VCP_chr9_35059798_ENST00000358901_length(amino acids)=466AA_BP=225
MLGEVTSQRDGGGSFRQLKGDLGPEDPSPSAAGRGQAGPVGAGAAAAALGLSHPPRIEALGAAGRQESDGESGAVRGAEPGAGPAVAAAA
APPPRVQTQEAAGRAGANRAAAAMELRVGNRYRLGRKIGSGSFGDIYLGTDIAAGEEVAIKLECVKTKHPQLHIESKIYKMMQGGVGIPT
IRWCGAEGDYNVMVMELLGPSLEDLFNFCSRKFSLKTVLLLADQMARQAAPCVLFFDELDSIAKARGGNIGDGGGAADRVINQILTEMDG
MSTKKNVFIIGATNRPDIIDPAILRPGRLDQLIYIPLPDEKSRVAILKANLRKSPVAKDVDLEFLAKMTNGFSGADLTEICQRACKLAIR
ESIESEIRRERERQTNPSAMEVEEDDPVPEIRRDHFEEAMRFARRSVSDNDIRKYEMFAQTLQQSRGFGSFRFPSGNQGGAGPSQGSGGG

--------------------------------------------------------------

>19827_19827_2_CSNK1D-VCP_CSNK1D_chr17_80213304_ENST00000398519_VCP_chr9_35059798_ENST00000358901_length(amino acids)=353AA_BP=112
MELRVGNRYRLGRKIGSGSFGDIYLGTDIAAGEEVAIKLECVKTKHPQLHIESKIYKMMQGGVGIPTIRWCGAEGDYNVMVMELLGPSLE
DLFNFCSRKFSLKTVLLLADQMARQAAPCVLFFDELDSIAKARGGNIGDGGGAADRVINQILTEMDGMSTKKNVFIIGATNRPDIIDPAI
LRPGRLDQLIYIPLPDEKSRVAILKANLRKSPVAKDVDLEFLAKMTNGFSGADLTEICQRACKLAIRESIESEIRRERERQTNPSAMEVE

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr17:80213304/chr9:35059798)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CSNK1D

P48730

.
FUNCTION: Essential serine/threonine-protein kinase that regulates diverse cellular growth and survival processes including Wnt signaling, DNA repair and circadian rhythms. It can phosphorylate a large number of proteins. Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. Phosphorylates connexin-43/GJA1, MAP1A, SNAPIN, MAPT/TAU, TOP2A, DCK, HIF1A, EIF6, p53/TP53, DVL2, DVL3, ESR1, AIB1/NCOA3, DNMT1, PKD2, YAP1, PER1 and PER2. Central component of the circadian clock. In balance with PP1, determines the circadian period length through the regulation of the speed and rhythmicity of PER1 and PER2 phosphorylation. Controls PER1 and PER2 nuclear transport and degradation. YAP1 phosphorylation promotes its SCF(beta-TRCP) E3 ubiquitin ligase-mediated ubiquitination and subsequent degradation. DNMT1 phosphorylation reduces its DNA-binding activity. Phosphorylation of ESR1 and AIB1/NCOA3 stimulates their activity and coactivation. Phosphorylation of DVL2 and DVL3 regulates WNT3A signaling pathway that controls neurite outgrowth. EIF6 phosphorylation promotes its nuclear export. Triggers down-regulation of dopamine receptors in the forebrain. Activates DCK in vitro by phosphorylation. TOP2A phosphorylation favors DNA cleavable complex formation. May regulate the formation of the mitotic spindle apparatus in extravillous trophoblast. Modulates connexin-43/GJA1 gap junction assembly by phosphorylation. Probably involved in lymphocyte physiology. Regulates fast synaptic transmission mediated by glutamate. {ECO:0000269|PubMed:10606744, ECO:0000269|PubMed:12270943, ECO:0000269|PubMed:14761950, ECO:0000269|PubMed:16027726, ECO:0000269|PubMed:17562708, ECO:0000269|PubMed:17962809, ECO:0000269|PubMed:19043076, ECO:0000269|PubMed:19339517, ECO:0000269|PubMed:20041275, ECO:0000269|PubMed:20048001, ECO:0000269|PubMed:20407760, ECO:0000269|PubMed:20637175, ECO:0000269|PubMed:20696890, ECO:0000269|PubMed:20699359, ECO:0000269|PubMed:21084295, ECO:0000269|PubMed:21422228, ECO:0000269|PubMed:23636092}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000314028-3915_23112.0416.0Nucleotide bindingATP
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000392334-31015_23112.0420.3333333333333Nucleotide bindingATP
TgeneVCPchr17:80213304chr9:35059798ENST000003589011217802_806565.0807.0MotifPIM motif

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000314028-399_277112.0416.0DomainProtein kinase
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000392334-3109_277112.0420.3333333333333DomainProtein kinase
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000314028-39278_364112.0416.0RegionNote=Centrosomal localization signal (CLS)
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000314028-39317_342112.0416.0RegionAutoinhibitory
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000392334-310278_364112.0420.3333333333333RegionNote=Centrosomal localization signal (CLS)
HgeneCSNK1Dchr17:80213304chr9:35059798ENST00000392334-310317_342112.0420.3333333333333RegionAutoinhibitory
TgeneVCPchr17:80213304chr9:35059798ENST000003589011217247_253565.0807.0Nucleotide bindingATP 1
TgeneVCPchr17:80213304chr9:35059798ENST000003589011217521_526565.0807.0Nucleotide bindingATP 2


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CSNK1D
VCP


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to CSNK1D-VCP


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to CSNK1D-VCP


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource