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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: 10418

FusionGeneSummary for DOCK8_GLIPR2

check button Fusion gene summary
Fusion gene informationFusion gene name: DOCK8_GLIPR2
Fusion gene ID: 10418
HgeneTgene
Gene symbol

DOCK8

GLIPR2

Gene ID

81704

152007

Gene namededicator of cytokinesis 8GLI pathogenesis related 2
SynonymsHEL-205|MRD2|ZIR8C9orf19|GAPR-1|GAPR1
Cytomap

9p24.3

9p13.3

Type of geneprotein-codingprotein-coding
Descriptiondedicator of cytokinesis protein 81200017A24Rikepididymis luminal protein 205Golgi-associated plant pathogenesis-related protein 117kD fetal brain proteingliPR 2glioma pathogenesis-related protein 2golgi-associated PR-1 protein
Modification date2018051920180523
UniProtAcc

Q8NF50

Q9H4G4

Ensembl transtripts involved in fusion geneENST00000453981, ENST00000432829, 
ENST00000469391, ENST00000382331, 
ENST00000382329, ENST00000493666, 
ENST00000396613, ENST00000377959, 
ENST00000377960, ENST00000474050, 
Fusion gene scores* DoF score3 X 3 X 3=279 X 4 X 5=180
# samples 37
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(7/180*10)=-1.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DOCK8 [Title/Abstract] AND GLIPR2 [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
HgeneDOCK8

GO:0043547

positive regulation of GTPase activity

28028151

TgeneGLIPR2

GO:0010634

positive regulation of epithelial cell migration

23516513

TgeneGLIPR2

GO:0010718

positive regulation of epithelial to mesenchymal transition

23516513

TgeneGLIPR2

GO:0070374

positive regulation of ERK1 and ERK2 cascade

23516513


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
TCGALDBRCATCGA-C8-A26Z-01ADOCK8chr9

449927

+GLIPR2chr9

36162359

+
* 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-3UTRENST00000453981ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000453981ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000453981ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000453981ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000432829ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000432829ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000432829ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000432829ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000469391ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000469391ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000469391ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000469391ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000382331ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000382331ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000382331ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000382331ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000382329ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000382329ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000382329ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
5CDS-3UTRENST00000382329ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000493666ENST00000396613DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000493666ENST00000377959DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000493666ENST00000377960DOCK8chr9

449927

+GLIPR2chr9

36162359

+
intron-3UTRENST00000493666ENST00000474050DOCK8chr9

449927

+GLIPR2chr9

36162359

+

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FusionProtFeatures for DOCK8_GLIPR2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DOCK8

Q8NF50

GLIPR2

Q9H4G4


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 DOCK8_GLIPR2


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 DOCK8_GLIPR2


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
DOCK8CDC42, RAC1, SMAD2, CRLF3, DOCK6, DOCK7, LRCH1, LRCH2, LRCH3, MOB1A, MOB1B, DGCR6, BYSL, HBZ, MEOX2, CARHSP1, CHMP2A, ZNF581, FBXL12, FANCL, EXOSC5, MRPL38, DOCK8, FAM161A, MED30, MTG1, KRT40, ZFC3H1, FAM124A, RTP5, ARPC3, PFKFB2, NSMAF, BAG3, MORC3, CDC5L, LRCH4, APPBP2, CPNE7GLIPR2ELAVL1, CDV3, SVIL, CAV1, PNMA5, KRTAP10-3, ANKRD12


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 DOCK8_GLIPR2


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 DOCK8_GLIPR2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDOCK8C0008073Developmental Disabilities1CTD_human
HgeneDOCK8C0027819Neuroblastoma1CTD_human
HgeneDOCK8C1968689Hyper-Immunoglobulin E Syndrome, Autosomal Recessive1ORPHANET;UNIPROT
HgeneDOCK8C3714756Intellectual Disability1CTD_human