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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:NIN-DOK3 (FusionGDB2 ID:59144)

Fusion Gene Summary for NIN-DOK3

check button Fusion gene summary
Fusion gene informationFusion gene name: NIN-DOK3
Fusion gene ID: 59144
HgeneTgene
Gene symbol

NIN

DOK3

Gene ID

51199

79930

Gene namenineindocking protein 3
SynonymsSCKL7DOKL
Cytomap

14q22.1

5q35.3

Type of geneprotein-codingprotein-coding
Descriptionnineinglycogen synthase kinase 3 beta-interacting proteinhNineinninein (GSK3B interacting protein)ninein centrosomal proteindocking protein 3Dok-like proteindownstream of tyrosine kinase 3
Modification date2020032820200313
UniProtAcc

Q8N4C6

Q7L591

Ensembl transtripts involved in fusion geneENST00000245441, ENST00000324330, 
ENST00000382041, ENST00000382043, 
ENST00000389868, ENST00000453196, 
ENST00000486200, ENST00000530997, 
ENST00000312943, ENST00000357198, 
ENST00000377112, ENST00000501403, 
Fusion gene scores* DoF score16 X 18 X 9=25921 X 1 X 1=1
# samples 201
** MAII scorelog2(20/2592*10)=-3.6959938131099
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: NIN [Title/Abstract] AND DOK3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNIN(51226826)-DOK3(176931206), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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 buttonFusion gene breakpoints across NIN (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across DOK3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABX644492NINchr14

51226826

-DOK3chr5

176931206

-


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Fusion Gene ORF analysis for NIN-DOK3

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-intronENST00000245441ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000245441ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000245441ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000245441ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000324330ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000324330ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000324330ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000324330ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382041ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382041ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382041ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382041ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382043ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382043ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382043ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000382043ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000389868ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000389868ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000389868ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000389868ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000453196ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000453196ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000453196ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000453196ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000486200ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000486200ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000486200ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000486200ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000530997ENST00000312943NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000530997ENST00000357198NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000530997ENST00000377112NINchr14

51226826

-DOK3chr5

176931206

-
intron-intronENST00000530997ENST00000501403NINchr14

51226826

-DOK3chr5

176931206

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for NIN-DOK3


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for NIN-DOK3


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:51226826/:176931206)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

Q8N4C6

DOK3

Q7L591

FUNCTION: Centrosomal protein required in the positioning and anchorage of the microtubule minus-end in epithelial cells (PubMed:15190203, PubMed:23386061). May also act as a centrosome maturation factor (PubMed:11956314). May play a role in microtubule nucleation, by recruiting the gamma-tubulin ring complex to the centrosome (PubMed:15190203). Overexpression does not perturb nucleation or elongation of microtubules but suppresses release of microtubules (PubMed:15190203). Required for centriole organization and microtubule anchoring at the mother centriole (PubMed:23386061). {ECO:0000269|PubMed:11956314, ECO:0000269|PubMed:15190203, ECO:0000269|PubMed:23386061}.FUNCTION: DOK proteins are enzymatically inert adaptor or scaffolding proteins. They provide a docking platform for the assembly of multimolecular signaling complexes. DOK3 is a negative regulator of JNK signaling in B-cells through interaction with INPP5D/SHIP1. May modulate ABL1 function (By similarity). {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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Fusion Gene Sequence for NIN-DOK3


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for NIN-DOK3


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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Related Drugs for NIN-DOK3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for NIN-DOK3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource