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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: 36673

FusionGeneSummary for STXBP1_SOX13

check button Fusion gene summary
Fusion gene informationFusion gene name: STXBP1_SOX13
Fusion gene ID: 36673
HgeneTgene
Gene symbol

STXBP1

SOX13

Gene ID

6812

9580

Gene namesyntaxin binding protein 1SRY-box 13
SynonymsMUNC18-1|NSEC1|P67|RBSEC1|UNC18ICA12|Sox-13
Cytomap

9q34.11

1q32.1

Type of geneprotein-codingprotein-coding
Descriptionsyntaxin-binding protein 1N-Sec1neuronal SEC1protein unc-18 homolog 1protein unc-18 homolog Aunc-18Aunc18-1transcription factor SOX-13SRY (sex determining region Y)-box 13SRY-related HMG-box gene 13islet cell antibody 12islet cell antigen 12type 1 diabetes autoantigen ICA12
Modification date2018052720180523
UniProtAcc

P61764

Q9UN79

Ensembl transtripts involved in fusion geneENST00000373302, ENST00000373299, 
ENST00000481942, 
ENST00000367203, 
ENST00000367204, 
Fusion gene scores* DoF score5 X 5 X 3=753 X 2 X 3=18
# samples 54
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: STXBP1 [Title/Abstract] AND SOX13 [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
HgeneSTXBP1

GO:0072659

protein localization to plasma membrane

17543282


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
TCGARVUCSTCGA-N8-A56S-01ASTXBP1chr9

130374719

+SOX13chr1

204082043

+
* 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
5CDS-3UTRENST00000373302ENST00000367203STXBP1chr9

130374719

+SOX13chr1

204082043

+
5CDS-5UTRENST00000373302ENST00000367204STXBP1chr9

130374719

+SOX13chr1

204082043

+
5CDS-3UTRENST00000373299ENST00000367203STXBP1chr9

130374719

+SOX13chr1

204082043

+
5CDS-5UTRENST00000373299ENST00000367204STXBP1chr9

130374719

+SOX13chr1

204082043

+
intron-3UTRENST00000481942ENST00000367203STXBP1chr9

130374719

+SOX13chr1

204082043

+
intron-5UTRENST00000481942ENST00000367204STXBP1chr9

130374719

+SOX13chr1

204082043

+

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FusionProtFeatures for STXBP1_SOX13


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
STXBP1

P61764

SOX13

Q9UN79

May participate in the regulation of synaptic vesicledocking and fusion, possibly through interaction with GTP-bindingproteins. Essential for neurotransmission and binds syntaxin, acomponent of the synaptic vesicle fusion machinery probably in a1:1 ratio. Can interact with syntaxins 1, 2, and 3 but notsyntaxin 4. May play a role in determining the specificity ofintracellular fusion reactions. Binds to the sequence 5'-AACAAT-3'. {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 STXBP1_SOX13


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 STXBP1_SOX13


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
STXBP1CDK5, MAPT, TUBB2A, TUBA4A, STX1A, STX2, STX4, SYTL4, STX1B, HGS, APP, KCTD3, IQCB1, SQSTM1, APBA1, APBA2, STX11, TRIM38, STX19, STX3, ARMC1, HAX1, NUFIP1, RRP7A, CDCA8, DGUOK, DNAAF2, GJA1, ACTR2, ARHGAP17, NPEPPS, PPP1R8, SHC1, SHMT1, ACTR3, ALDOC, ARPC3, EHD1, NDUFV1, NUP50, PICALM, SNAP25, NTRK1, PRKCA, ID1, POLG2, DNAJC11, FERMT3, SPTBN1, TUSC3, TM4SF18, GPRC5B, MTNR1ASOX13SOX13, SMAD7, CTBP2, YTHDC1, CLEC12A, CEP85, XPO1, SOX5, TRIM25


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 STXBP1_SOX13


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 STXBP1_SOX13


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSTXBP1C2677326Epileptic Encephalopathy, Early Infantile, 45CTD_human;UNIPROT
HgeneSTXBP1C0014550Epilepsies, Myoclonic1CTD_human;HPO
HgeneSTXBP1C0036341Schizophrenia1PSYGENET