FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 10538

FusionGeneSummary for DPYSL2_SPIN1

check button Fusion gene summary
Fusion gene informationFusion gene name: DPYSL2_SPIN1
Fusion gene ID: 10538
HgeneTgene
Gene symbol

DPYSL2

SPIN1

Gene ID

1808

83985

Gene namedihydropyrimidinase like 2sphingolipid transporter 1 (putative)
SynonymsCRMP-2|CRMP2|DHPRP2|DRP-2|DRP2|N2A3|ULIP-2|ULIP2HSpin1|LAT|PP2030|SPIN1|SPINL|nrs
Cytomap

8p21.2

16p11.2

Type of geneprotein-codingprotein-coding
Descriptiondihydropyrimidinase-related protein 2collapsin response mediator protein hCRMP-2unc-33-like phosphoprotein 2protein spinster homolog 1SPNS sphingolipid transporter 1 (putative)spinster homolog 1spinster-like protein 1
Modification date2018051920180522
UniProtAcc

Q16555

Q9Y657

Ensembl transtripts involved in fusion geneENST00000521913, ENST00000311151, 
ENST00000523027, ENST00000521983, 
ENST00000375859, ENST00000541629, 
ENST00000469017, 
Fusion gene scores* DoF score9 X 7 X 3=1895 X 6 X 1=30
# samples 96
** MAII scorelog2(9/189*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/30*10)=1
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: DPYSL2 [Title/Abstract] AND SPIN1 [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

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
ChiTaRS3.1AW889897DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
* 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
3UTR-3UTRENST00000521913ENST00000375859DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
3UTR-intronENST00000521913ENST00000541629DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
3UTR-intronENST00000521913ENST00000469017DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
3UTR-3UTRENST00000311151ENST00000375859DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
3UTR-intronENST00000311151ENST00000541629DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
3UTR-intronENST00000311151ENST00000469017DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-3UTRENST00000523027ENST00000375859DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-intronENST00000523027ENST00000541629DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-intronENST00000523027ENST00000469017DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-3UTRENST00000521983ENST00000375859DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-intronENST00000521983ENST00000541629DPYSL2chr8

26515291

-SPIN1chr9

91092895

+
intron-intronENST00000521983ENST00000469017DPYSL2chr8

26515291

-SPIN1chr9

91092895

+

Top

FusionProtFeatures for DPYSL2_SPIN1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DPYSL2

Q16555

SPIN1

Q9Y657

Plays a role in neuronal development and polarity, aswell as in axon growth and guidance, neuronal growth cone collapseand cell migration. Necessary for signaling by class 3 semaphorinsand subsequent remodeling of the cytoskeleton. May play a role inendocytosis. {ECO:0000269|PubMed:11477421,ECO:0000269|PubMed:15466863, ECO:0000269|PubMed:20801876}. Chromatin reader that specifically recognizes and bindshistone H3 both trimethylated at 'Lys-4' and asymmetricallydimethylated at 'Arg-8' (H3K4me3 and H3R8me2a) and acts as anactivator of Wnt signaling pathway downstream of PRMT2. In case ofcancer, promotes cell cancer proliferation via activation of theWnt signaling pathway (PubMed:24589551). Overexpression inducesmetaphase arrest and chromosomal instability. Localizes to activerDNA loci and promotes the expression of rRNA genes(PubMed:21960006). May play a role in cell-cycle regulation duringthe transition from gamete to embryo. Involved in oocyte meioticresumption, a process that takes place before ovulation to resumemeiosis of oocytes blocked in prophase I: may act by regulatingmaternal transcripts to control meiotic resumption.{ECO:0000269|PubMed:21960006, ECO:0000269|PubMed:22258766,ECO:0000269|PubMed:24589551, ECO:0000269|PubMed:29061846}.

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


Top

FusionGeneSequence for DPYSL2_SPIN1


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).

Top

FusionGenePPI for DPYSL2_SPIN1


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


Top

RelatedDrugs for DPYSL2_SPIN1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneDPYSL2Q16555DB11638ArtenimolDihydropyrimidinase-related protein 2small moleculeapproved|investigational

Top

RelatedDiseases for DPYSL2_SPIN1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDPYSL2C0005586Bipolar Disorder4PSYGENET
HgeneDPYSL2C0001973Alcoholic Intoxication, Chronic1PSYGENET
HgeneDPYSL2C0002395Alzheimer's Disease1CTD_human
HgeneDPYSL2C0011570Mental Depression1PSYGENET
HgeneDPYSL2C0011581Depressive disorder1PSYGENET
HgeneDPYSL2C0029408Degenerative polyarthritis1CTD_human
HgeneDPYSL2C0033937Psychoses, Drug1PSYGENET
HgeneDPYSL2C0036349Paranoid Schizophrenia1CTD_human