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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: 41812

FusionGeneSummary for WDR1_STX4

check button Fusion gene summary
Fusion gene informationFusion gene name: WDR1_STX4
Fusion gene ID: 41812
HgeneTgene
Gene symbol

WDR1

STX4

Gene ID

9948

6810

Gene nameWD repeat domain 1syntaxin 4
SynonymsAIP1|HEL-S-52|NORI-1STX4A|p35-2
Cytomap

4p16.1

16p11.2

Type of geneprotein-codingprotein-coding
DescriptionWD repeat-containing protein 1actin-interacting protein 1epididymis secretory protein Li 52syntaxin-4renal carcinoma antigen NY-REN-31syntaxin 4A (placental)
Modification date2018052320180523
UniProtAcc

O75083

Q12846

Ensembl transtripts involved in fusion geneENST00000499869, ENST00000382451, 
ENST00000382452, ENST00000515743, 
ENST00000502702, 
ENST00000493902, 
ENST00000394998, ENST00000313843, 
Fusion gene scores* DoF score4 X 7 X 2=562 X 2 X 1=4
# samples 72
** MAII scorelog2(7/56*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/4*10)=2.32192809488736
Context

PubMed: WDR1 [Title/Abstract] AND STX4 [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
HgeneWDR1

GO:0030834

regulation of actin filament depolymerization

15629458

HgeneWDR1

GO:0043297

apical junction assembly

25792565

HgeneWDR1

GO:0045199

maintenance of epithelial cell apical/basal polarity

25792565

TgeneSTX4

GO:0033194

response to hydroperoxide

22226963

TgeneSTX4

GO:0035774

positive regulation of insulin secretion involved in cellular response to glucose stimulus

24552216

TgeneSTX4

GO:0048284

organelle fusion

20434989

TgeneSTX4

GO:0060291

long-term synaptic potentiation

20434989


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
ChiTaRS3.1BQ346391WDR1chr4

10087865

+STX4chr16

31045423

-
* 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
intron-3UTRENST00000499869ENST00000493902WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000499869ENST00000394998WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000499869ENST00000313843WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382451ENST00000493902WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382451ENST00000394998WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382451ENST00000313843WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382452ENST00000493902WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382452ENST00000394998WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000382452ENST00000313843WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000515743ENST00000493902WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000515743ENST00000394998WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000515743ENST00000313843WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000502702ENST00000493902WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000502702ENST00000394998WDR1chr4

10087865

+STX4chr16

31045423

-
intron-3UTRENST00000502702ENST00000313843WDR1chr4

10087865

+STX4chr16

31045423

-

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FusionProtFeatures for WDR1_STX4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
WDR1

O75083

STX4

Q12846

Induces disassembly of actin filaments in conjunctionwith ADF/cofilin family proteins (PubMed:15629458). Enhancescofilin-mediated actin severing (By similarity). Involved incytokinesis. Involved in chemotactic cell migration by restrictinglamellipodial membrane protrusions (PubMed:18494608). Involved inmyocardium sarcomere organization. Required for cardiomyocytegrowth and maintenance (By similarity). Involved in megakaryocytematuration and platelet shedding. Required for the establishmentof planar cell polarity (PCP) during follicular epitheliumdevelopment and for cell shape changes during PCP; the functionseems to implicate cooperation with CFL1 and/or DSTN/ADF. Involvedin the generation/maintenance of cortical tension (By similarity).Involved in assembly and maintenance of epithelial apical celljunctions and plays a role in the organization of theperijunctional actomyosin belt (PubMed:25792565).{ECO:0000250|UniProtKB:O88342, ECO:0000250|UniProtKB:Q9W7F2,ECO:0000269|PubMed:15629458, ECO:0000269|PubMed:18494608,ECO:0000269|PubMed:25792565}. Plasma membrane t-SNARE that mediates docking oftransport vesicles. Necessary for the translocation of SLC2A4 fromintracellular vesicles to the plasma membrane. Together with STXB3and VAMP2, may also play a role in docking/fusion of intracellularGLUT4-containing vesicles with the cell surface in adipocytes (Bysimilarity). May also play a role in docking of synaptic vesiclesat presynaptic active zones. {ECO:0000250}.

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 WDR1_STX4


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 WDR1_STX4


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


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 WDR1_STX4


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 WDR1_STX4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneWDR1C0021368Inflammation1CTD_human
HgeneWDR1C0029456Osteoporosis1CTD_human
HgeneWDR1C0040034Thrombocytopenia1CTD_human