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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:DOCK7-NMT2 (FusionGDB2 ID:23812)

Fusion Gene Summary for DOCK7-NMT2

check button Fusion gene summary
Fusion gene informationFusion gene name: DOCK7-NMT2
Fusion gene ID: 23812
HgeneTgene
Gene symbol

DOCK7

NMT2

Gene ID

85440

9397

Gene namededicator of cytokinesis 7N-myristoyltransferase 2
SynonymsEIEE23|ZIR2-
Cytomap

1p31.3

10p13

Type of geneprotein-codingprotein-coding
Descriptiondedicator of cytokinesis protein 7glycylpeptide N-tetradecanoyltransferase 2NMT 2glycylpeptide N-tetradecanoyltransferase 2 variant 3glycylpeptide N-tetradecanoyltransferase 2 variant 4myristoyl-CoA:protein N-myristoyltransferase 2peptide N-myristoyltransferase 2type II N-myristoylt
Modification date2020032720200313
UniProtAcc

Q96N67

O60551

Ensembl transtripts involved in fusion geneENST00000251157, ENST00000340370, 
ENST00000489185, ENST00000404627, 
ENST00000378165, ENST00000378150, 
ENST00000535341, ENST00000466201, 
ENST00000540259, 
Fusion gene scores* DoF score13 X 12 X 7=10924 X 3 X 4=48
# samples 145
** MAII scorelog2(14/1092*10)=-2.96347412397489
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: DOCK7 [Title/Abstract] AND NMT2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDOCK7(63153898)-NMT2(15183556), # samples:2
Anticipated loss of major functional domain due to fusion event.DOCK7-NMT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
* 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
HgeneDOCK7

GO:0090630

activation of GTPase activity

16982419

TgeneNMT2

GO:0018008

N-terminal peptidyl-glycine N-myristoylation

25255805


check buttonFusion gene breakpoints across DOCK7 (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 NMT2 (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
ChimerDB4SARCTCGA-IF-A4AK-01ADOCK7chr1

63153898

-NMT2chr10

15183556

-
ChimerDB4SARCTCGA-IF-A4AKDOCK7chr1

63153897

-NMT2chr10

15183556

-
ChimerDB4SARCTCGA-IF-A4AK-01ADOCK7chr1

63153898

-NMT2chr10

15183556

-


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Fusion Gene ORF analysis for DOCK7-NMT2

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-shiftENST00000251157ENST00000378165DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000251157ENST00000378150DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000251157ENST00000535341DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-intronENST00000251157ENST00000466201DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-5UTRENST00000251157ENST00000540259DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000378165DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000378150DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000535341DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-intronENST00000340370ENST00000466201DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-5UTRENST00000340370ENST00000540259DOCK7chr1

63153898

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000378165DOCK7chr1

63153898

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000378150DOCK7chr1

63153898

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000535341DOCK7chr1

63153898

-NMT2chr10

15183556

-
intron-intronENST00000489185ENST00000466201DOCK7chr1

63153898

-NMT2chr10

15183556

-
intron-5UTRENST00000489185ENST00000540259DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000378165DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000378150DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000535341DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-intronENST00000404627ENST00000466201DOCK7chr1

63153898

-NMT2chr10

15183556

-
5CDS-5UTRENST00000404627ENST00000540259DOCK7chr1

63153898

-NMT2chr10

15183556

-
Frame-shiftENST00000251157ENST00000378165DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000251157ENST00000378150DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000251157ENST00000535341DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-intronENST00000251157ENST00000466201DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-5UTRENST00000251157ENST00000540259DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000378165DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000378150DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000340370ENST00000535341DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-intronENST00000340370ENST00000466201DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-5UTRENST00000340370ENST00000540259DOCK7chr1

63153897

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000378165DOCK7chr1

63153897

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000378150DOCK7chr1

63153897

-NMT2chr10

15183556

-
intron-3CDSENST00000489185ENST00000535341DOCK7chr1

63153897

-NMT2chr10

15183556

-
intron-intronENST00000489185ENST00000466201DOCK7chr1

63153897

-NMT2chr10

15183556

-
intron-5UTRENST00000489185ENST00000540259DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000378165DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000378150DOCK7chr1

63153897

-NMT2chr10

15183556

-
Frame-shiftENST00000404627ENST00000535341DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-intronENST00000404627ENST00000466201DOCK7chr1

63153897

-NMT2chr10

15183556

-
5CDS-5UTRENST00000404627ENST00000540259DOCK7chr1

63153897

-NMT2chr10

15183556

-

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 DOCK7-NMT2


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 DOCK7-NMT2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DOCK7

Q96N67

NMT2

O60551

FUNCTION: Functions as a guanine nucleotide exchange factor (GEF), which activates Rac1 and Rac3 Rho small GTPases by exchanging bound GDP for free GTP. Does not have a GEF activity for CDC42. Required for STMN1 'Ser-15' phosphorylation during axon formation and consequently for neuronal polarization (PubMed:16982419). As part of the DISP complex, may regulate the association of septins with actin and thereby regulate the actin cytoskeleton (PubMed:29467281). Has a role in pigmentation (By similarity). Involved in the regulation of cortical neurogenesis through the control of radial glial cells (RGCs) proliferation versus differentiation; negatively regulates the basal-to-apical interkinetic nuclear migration of RGCs by antagonizing the microtubule growth-promoting function of TACC3 (By similarity). {ECO:0000250|UniProtKB:Q8R1A4, ECO:0000269|PubMed:16982419, ECO:0000269|PubMed:29467281}.FUNCTION: Adds a myristoyl group to the N-terminal glycine residue of certain cellular and viral proteins. {ECO:0000269|PubMed:25255805, ECO:0000269|PubMed:9506952}.

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 DOCK7-NMT2


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 DOCK7-NMT2


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 DOCK7-NMT2


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 DOCK7-NMT2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDOCK7C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneDOCK7C4014492EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 231CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneNMT2C0010093Corpus Luteum Cyst1CTD_human
TgeneNMT2C0029927Ovarian Cysts1CTD_human