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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: 10403

FusionGeneSummary for DOCK4_TPH2

check button Fusion gene summary
Fusion gene informationFusion gene name: DOCK4_TPH2
Fusion gene ID: 10403
HgeneTgene
Gene symbol

DOCK4

TPH2

Gene ID

9732

121278

Gene namededicator of cytokinesis 4tryptophan hydroxylase 2
Synonyms-ADHD7|NTPH
Cytomap

7q31.1

12q21.1

Type of geneprotein-codingprotein-coding
Descriptiondedicator of cytokinesis protein 4tryptophan 5-hydroxylase 2neuronal tryptophan hydroxylasetryptophan 5-monooxygenase 2
Modification date2018052520180522
UniProtAcc

Q8N1I0

Q8IWU9

Ensembl transtripts involved in fusion geneENST00000428084, ENST00000494651, 
ENST00000437633, ENST00000476846, 
ENST00000333850, ENST00000546576, 
Fusion gene scores* DoF score6 X 2 X 5=605 X 4 X 3=60
# samples 64
** MAII scorelog2(6/60*10)=0log2(4/60*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DOCK4 [Title/Abstract] AND TPH2 [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
TCGARVCESCTCGA-FU-A3TX-01ADOCK4chr7

111846157

-TPH2chr12

72366299

+
* 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-shiftENST00000428084ENST00000333850DOCK4chr7

111846157

-TPH2chr12

72366299

+
5CDS-intronENST00000428084ENST00000546576DOCK4chr7

111846157

-TPH2chr12

72366299

+
intron-3CDSENST00000494651ENST00000333850DOCK4chr7

111846157

-TPH2chr12

72366299

+
intron-intronENST00000494651ENST00000546576DOCK4chr7

111846157

-TPH2chr12

72366299

+
Frame-shiftENST00000437633ENST00000333850DOCK4chr7

111846157

-TPH2chr12

72366299

+
5CDS-intronENST00000437633ENST00000546576DOCK4chr7

111846157

-TPH2chr12

72366299

+
5UTR-3CDSENST00000476846ENST00000333850DOCK4chr7

111846157

-TPH2chr12

72366299

+
5UTR-intronENST00000476846ENST00000546576DOCK4chr7

111846157

-TPH2chr12

72366299

+

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FusionProtFeatures for DOCK4_TPH2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DOCK4

Q8N1I0

TPH2

Q8IWU9

Involved in regulation of adherens junction betweencells. Plays a role in cell migration. Functions as a guaninenucleotide exchange factor (GEF), which activates Rap1 smallGTPase by exchanging bound GDP for free GTP.{ECO:0000269|PubMed:12628187, ECO:0000269|PubMed:20679435}.

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 DOCK4_TPH2


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 DOCK4_TPH2


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
DOCK4HNRNPL, YWHAB, RNF115, FASLG, GRK5, EGFR, EIF4A3, MAGOH, GRB2, NPM1, ELMO1, NTRK1, ELMO3, ARRB1, ERMAP, STAT1, VSIG8TPH2DNAJC12, SYBU


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 DOCK4_TPH2


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 DOCK4_TPH2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDOCK4C0036341Schizophrenia2PSYGENET
HgeneDOCK4C0004352Autistic Disorder1CTD_human
TgeneTPH2C0011581Depressive disorder6CTD_human;PSYGENET
TgeneTPH2C0005586Bipolar Disorder5PSYGENET
TgeneTPH2C0011570Mental Depression5PSYGENET
TgeneTPH2C0041696Unipolar Depression5PSYGENET
TgeneTPH2C0525045Mood Disorders5PSYGENET
TgeneTPH2C1269683Major Depressive Disorder5CTD_human;PSYGENET
TgeneTPH2C0033975Psychotic Disorders2PSYGENET
TgeneTPH2C0036341Schizophrenia2PSYGENET
TgeneTPH2C0600427Cocaine Dependence2PSYGENET
TgeneTPH2C0001956alcohol use disorder1PSYGENET
TgeneTPH2C0004352Autistic Disorder1CTD_human
TgeneTPH2C0005587Depression, Bipolar1PSYGENET
TgeneTPH2C0015967Fever1CTD_human
TgeneTPH2C0036349Paranoid Schizophrenia1PSYGENET
TgeneTPH2C0038586Substance Use Disorders1PSYGENET
TgeneTPH2C0085762Alcohol abuse1PSYGENET
TgeneTPH2C0338715Drug-induced depressive state1PSYGENET
TgeneTPH2C2751802ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 71UNIPROT