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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: 43702

FusionGeneSummary for ZNF785_DCX

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF785_DCX
Fusion gene ID: 43702
HgeneTgene
Gene symbol

ZNF785

DCX

Gene ID

146540

1641

Gene namezinc finger protein 785doublecortin
Synonyms-DBCN|DC|LISX|SCLH|XLIS
Cytomap

16p11.2

Xq23

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 785neuronal migration protein doublecortindoublecortexdoublinlis-Xlissencephalin-X
Modification date2018051920180523
UniProtAcc

A8K8V0

O43602

Ensembl transtripts involved in fusion geneENST00000470110, ENST00000395216, 
ENST00000371993, ENST00000356915, 
ENST00000338081, ENST00000356220, 
ENST00000488120, ENST00000496551, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: ZNF785 [Title/Abstract] AND DCX [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
TgeneDCX

GO:0001764

neuron migration

14741102


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
ChiTaRS3.1BM678941ZNF785chr16

30590845

+DCXchrX

110539882

+
* 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-3UTRENST00000470110ENST00000371993ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-3UTRENST00000470110ENST00000356915ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-3UTRENST00000470110ENST00000338081ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000470110ENST00000356220ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000470110ENST00000488120ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000470110ENST00000496551ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-3UTRENST00000395216ENST00000371993ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-3UTRENST00000395216ENST00000356915ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-3UTRENST00000395216ENST00000338081ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000395216ENST00000356220ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000395216ENST00000488120ZNF785chr16

30590845

+DCXchrX

110539882

+
intron-intronENST00000395216ENST00000496551ZNF785chr16

30590845

+DCXchrX

110539882

+

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FusionProtFeatures for ZNF785_DCX


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF785

A8K8V0

DCX

O43602

May be involved in transcriptional regulation.{ECO:0000250}. Microtubule-associated protein required for initialsteps of neuronal dispersion and cortex lamination during cerebralcortex development. May act by competing with the putativeneuronal protein kinase DCLK1 in binding to a target protein. Mayin that way participate in a signaling pathway that is crucial forneuronal interaction before and during migration, possibly as partof a calcium ion-dependent signal transduction pathway. May bepart with PAFAH1B1/LIS-1 of overlapping, but distinct, signalingpathways that promote neuronal migration.{ECO:0000269|PubMed:22359282}.

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 ZNF785_DCX


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 ZNF785_DCX


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 ZNF785_DCX


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 ZNF785_DCX


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDCXC1848199X-Linked Lissencephaly11ORPHANET;UNIPROT