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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 28755

FusionGeneSummary for PRKCI_TNIK

check button Fusion gene summary
Fusion gene informationFusion gene name: PRKCI_TNIK
Fusion gene ID: 28755
HgeneTgene
Gene symbol

PRKCI

TNIK

Gene ID

5584

23043

Gene nameprotein kinase C iotaTRAF2 and NCK interacting kinase
SynonymsDXS1179E|PKCI|nPKC-iotaMRT54
Cytomap

3q26.2

3q26.2-q26.31

Type of geneprotein-codingprotein-coding
Descriptionprotein kinase C iota typePRKC-lambda/iotaaPKC-lambda/iotaatypical protein kinase C-lambda/iotaTRAF2 and NCK-interacting protein kinase
Modification date2018052320180523
UniProtAcc

P41743

Q9UKE5

Ensembl transtripts involved in fusion geneENST00000295797, ENST00000436636, 
ENST00000538048, ENST00000369326, 
ENST00000341852, ENST00000284483, 
ENST00000470834, ENST00000460047, 
ENST00000475336, ENST00000488470, 
ENST00000357327, ENST00000464785, 
ENST00000465393, 
Fusion gene scores* DoF score6 X 5 X 4=1205 X 5 X 3=75
# samples 65
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PRKCI [Title/Abstract] AND TNIK [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgenePRKCI

GO:0006468

protein phosphorylation

8226978

HgenePRKCI

GO:0018105

peptidyl-serine phosphorylation

21983565

HgenePRKCI

GO:0043524

negative regulation of neuron apoptotic process

10467349

HgenePRKCI

GO:0051092

positive regulation of NF-kappaB transcription factor activity

10467349

TgeneTNIK

GO:0006468

protein phosphorylation

10521462|15342639|22797597

TgeneTNIK

GO:0007256

activation of JNKK activity

15342639

TgeneTNIK

GO:0031532

actin cytoskeleton reorganization

15342639

TgeneTNIK

GO:0035556

intracellular signal transduction

10521462

TgeneTNIK

GO:0046777

protein autophosphorylation

10521462|15342639

TgeneTNIK

GO:0048814

regulation of dendrite morphogenesis

20159449


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVBRCATCGA-D8-A27N-01APRKCIchr3

169953139

+TNIKchr3

170912424

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000295797ENST00000436636PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000538048PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000369326PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000341852PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000284483PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000470834PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000460047PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000475336PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000488470PRKCIchr3

169953139

+TNIKchr3

170912424

-
Frame-shiftENST00000295797ENST00000357327PRKCIchr3

169953139

+TNIKchr3

170912424

-
5CDS-intronENST00000295797ENST00000464785PRKCIchr3

169953139

+TNIKchr3

170912424

-
5CDS-intronENST00000295797ENST00000465393PRKCIchr3

169953139

+TNIKchr3

170912424

-

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FusionProtFeatures for PRKCI_TNIK


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

P41743

TNIK

Q9UKE5

Calcium- and diacylglycerol-independent serine/threonine-protein kinase that plays a general protective roleagainst apoptotic stimuli, is involved in NF-kappa-B activation,cell survival, differentiation and polarity, and contributes tothe regulation of microtubule dynamics in the early secretorypathway. Is necessary for BCR-ABL oncogene-mediated resistance toapoptotic drug in leukemia cells, protecting leukemia cellsagainst drug-induced apoptosis. In cultured neurons, preventsamyloid beta protein-induced apoptosis by interrupting cell deathprocess at a very early step. In glioblastoma cells, may functiondownstream of phosphatidylinositol 3-kinase (PI(3)K) and PDPK1 inthe promotion of cell survival by phosphorylating and inhibitingthe pro-apoptotic factor BAD. Can form a protein complex in non-small cell lung cancer (NSCLC) cells with PARD6A and ECT2 andregulate ECT2 oncogenic activity by phosphorylation, which in turnpromotes transformed growth and invasion. In response to nervegrowth factor (NGF), acts downstream of SRC to phosphorylate andactivate IRAK1, allowing the subsequent activation of NF-kappa-Band neuronal cell survival. Functions in the organization of theapical domain in epithelial cells by phosphorylating EZR. Thisstep is crucial for activation and normal distribution of EZR atthe early stages of intestinal epithelial cell differentiation.Forms a protein complex with LLGL1 and PARD6B independently ofPARD3 to regulate epithelial cell polarity. Plays a role inmicrotubule dynamics in the early secretory pathway throughinteraction with RAB2A and GAPDH and recruitment to vesiculartubular clusters (VTCs). In human coronary artery endothelialcells (HCAEC), is activated by saturated fatty acids and mediateslipid-induced apoptosis. {ECO:0000269|PubMed:10356400,ECO:0000269|PubMed:10467349, ECO:0000269|PubMed:10906326,ECO:0000269|PubMed:11042363, ECO:0000269|PubMed:11724794,ECO:0000269|PubMed:12871960, ECO:0000269|PubMed:14684752,ECO:0000269|PubMed:15994303, ECO:0000269|PubMed:18270268,ECO:0000269|PubMed:19327373, ECO:0000269|PubMed:21189248,ECO:0000269|PubMed:21419810, ECO:0000269|PubMed:8226978,ECO:0000269|PubMed:9346882}.

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for PRKCI_TNIK


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for PRKCI_TNIK


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
PRKCIPDPK1, PARD6A, BAD, ADAP1, YWHAZ, RAB4A, SQSTM1, SMG1, GAPDH, PARD3, FRS2, USP21, MARK2, GABARAPL1, GABARAPL2, MAP1LC3A, MAP1LC3B, SFPQ, VHL, CHUK, IKBKB, DUSP1, YWHAH, MARK4, PARD6B, PARD6G, GBAS, LLGL1, HSP90AA1, LLGL2, CDC37, NIPSNAP1, RAPGEF2, MYO10, PNMA1, FABP4, TTR, TSC22D1, MBP, CDK7, ELAVL1, TJP1, ARHGAP17, MAP2K5, APP, YWHAE, GAB1, NPM1, CRX, CASP8, IL1RAP, IKBKG, AMOT, PRKCZ, RHOJ, RASSF8, KIF23, PPM1A, PPM1B, CEP135, TMEM17, XPO1, SSB, MAGED2, ZNF609, TMEM208, EIF4ENIF1, TRAPPC13, MASTL, SMURF1, MTMR4, FYN, NGEF, KBTBD7, GPR156, FARP2, CD44, FGB, ARHGEF16, KERA, PDGFD, UBC, DCAF7, TRIM25, WWC1TNIKTRAF2, NEDD4, DISC1, DST, SYNE1, TNKS, SOS1, SPTBN1, MACF1, PDE4DIP, GOLGA4, SRGAP3, ANK2, TRIM2, DPYSL3, HARS, WWC1, TIAM2, TUBB2A, AKAP9, CLU, DPYSL2, NEFM, AGTPBP1, CNKSR2, NCOR2, DYNC1H1, PPP1R13B, SNX6, GSE1, ACTG1, PAFAH1B1, PPM1E, SMARCE1, NCK2, LTBR, CEP63, TMEM17, XPO1, SMURF1, EGFR, KBTBD7, IL20RA, MRPS11, UBE2A, TRAF6, MAP3K7, TAB2, IKBKB


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for PRKCI_TNIK


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for PRKCI_TNIK


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePRKCIC0005586Bipolar Disorder2PSYGENET
HgenePRKCIC0011570Mental Depression1PSYGENET
HgenePRKCIC0011581Depressive disorder1PSYGENET
TgeneTNIKC0036341Schizophrenia1PSYGENET
TgeneTNIKC0037274Dermatologic disorders1CTD_human
TgeneTNIKC0311375Arsenic Poisoning1CTD_human
TgeneTNIKC3495559Juvenile arthritis1CTD_human