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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:LUC7L-NME4 (FusionGDB2 ID:50371)

Fusion Gene Summary for LUC7L-NME4

check button Fusion gene summary
Fusion gene informationFusion gene name: LUC7L-NME4
Fusion gene ID: 50371
HgeneTgene
Gene symbol

LUC7L

NME4

Gene ID

55692

4833

Gene nameLUC7 likeNME/NM23 nucleoside diphosphate kinase 4
SynonymsLUC7B1|Luc7|SR+89|hLuc7B1NDPK-D|NM23H4|nm23-H4
Cytomap

16p13.3

16p13.3

Type of geneprotein-codingprotein-coding
Descriptionputative RNA-binding protein Luc7-like 1putative SR protein LUC7B1sarcoplasmic reticulum protein LUC7B1nucleoside diphosphate kinase, mitochondrialNDKNDP kinase DNDP kinase, mitochondrialNDPKDnon-metastatic cells 4, protein expressed innucleoside diphosphate kinase D
Modification date2020032020200313
UniProtAcc

Q9NQ29

O00746

Ensembl transtripts involved in fusion geneENST00000293872, ENST00000337351, 
ENST00000397783, ENST00000397780, 
ENST00000494366, 
ENST00000219479, 
ENST00000382940, ENST00000397722, 
ENST00000450036, 
Fusion gene scores* DoF score19 X 17 X 10=32304 X 3 X 5=60
# samples 255
** MAII scorelog2(25/3230*10)=-3.6915341649192
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LUC7L [Title/Abstract] AND NME4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointLUC7L(279277)-NME4(448989), # 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
TgeneNME4

GO:0006869

lipid transport

23150663


check buttonFusion gene breakpoints across LUC7L (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 NME4 (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
ChimerDB4OVTCGA-13-0899LUC7Lchr16

279277

-NME4chr16

448989

+


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Fusion Gene ORF analysis for LUC7L-NME4

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-5UTRENST00000293872ENST00000219479LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000293872ENST00000382940LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000293872ENST00000397722LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000293872ENST00000450036LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000337351ENST00000219479LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000337351ENST00000382940LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000337351ENST00000397722LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000337351ENST00000450036LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000397783ENST00000219479LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000397783ENST00000382940LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000397783ENST00000397722LUC7Lchr16

279277

-NME4chr16

448989

+
5CDS-5UTRENST00000397783ENST00000450036LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000397780ENST00000219479LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000397780ENST00000382940LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000397780ENST00000397722LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000397780ENST00000450036LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000494366ENST00000219479LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000494366ENST00000382940LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000494366ENST00000397722LUC7Lchr16

279277

-NME4chr16

448989

+
intron-5UTRENST00000494366ENST00000450036LUC7Lchr16

279277

-NME4chr16

448989

+

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 LUC7L-NME4


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)
LUC7Lchr16279277-NME4chr16448989+6.16E-101
LUC7Lchr16279277-NME4chr16448989+6.16E-101

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.
genomic feature of top 1%

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Fusion Protein Features for LUC7L-NME4


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/:279277/:448989)
- 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
LUC7L

Q9NQ29

NME4

O00746

FUNCTION: May bind to RNA via its Arg/Ser-rich domain. {ECO:0000269|PubMed:11170747}.FUNCTION: Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. Through the catalyzed exchange of gamma-phosphate between di- and triphosphonucleosides participates in regulation of intracellular nucleotide homeostasis (PubMed:10799505). Binds to anionic phospholipids, predominantly to cardiolipin; the binding inhibits its phosphotransfer activity (PubMed:18635542, PubMed:23150663). Acts as mitochondria-specific NDK; its association with cardiolipin-containing mitochondrial inner membrane is coupled to respiration suggesting that ADP locally regenerated in the mitochondrion innermembrane space by its activity is directly taken up via ANT ADP/ATP translocase into the matrix space to stimulate respiratory ATP regeneration (PubMed:18635542). Proposed to increase GTP-loading on dynamin-related GTPase OPA1 in mitochondria (PubMed:24970086). In vitro can induce liposome cross-linking suggesting that it can cross-link inner and outer membranes to form contact sites, and promotes intermembrane migration of anionic phosphoplipids. Promotes the redistribution of cardiolipin between the mitochondrial inner membrane and outer membrane which is implicated in pro-apoptotic signaling (PubMed:18635542, PubMed:17028143, PubMed:23150663). {ECO:0000269|PubMed:10799505, ECO:0000269|PubMed:17028143, ECO:0000269|PubMed:18635542, ECO:0000269|PubMed:23150663, ECO:0000305, ECO:0000305|PubMed:24970086}.

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 LUC7L-NME4


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 LUC7L-NME4


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 LUC7L-NME4


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 LUC7L-NME4


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