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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:TUBB2B-NME2 (FusionGDB2 ID:94689)

Fusion Gene Summary for TUBB2B-NME2

check button Fusion gene summary
Fusion gene informationFusion gene name: TUBB2B-NME2
Fusion gene ID: 94689
HgeneTgene
Gene symbol

TUBB2B

NME2

Gene ID

347733

4831

Gene nametubulin beta 2B class IIbNME/NM23 nucleoside diphosphate kinase 2
SynonymsCDCBM7|PMGYSA|bA506K6.1NDKB|NDPK-B|NDPKB|NM23-H2|NM23B|PUF
Cytomap

6p25.2

17q21.33

Type of geneprotein-codingprotein-coding
Descriptiontubulin beta-2B chainclass II beta-tubulin isotypeclass IIb beta-tubulinepididymis secretory sperm binding proteintubulin, beta 2Btubulin, beta polypeptide paralognucleoside diphosphate kinase BHEL-S-155anNDP kinase Bc-myc purine-binding transcription factor PUFc-myc transcription factorepididymis secretory sperm binding protein Li 155anhistidine protein kinase NDKBnon-metastatic cells 2, protein (NM23) expr
Modification date2020032020200327
UniProtAcc.

O60361

Ensembl transtripts involved in fusion geneENST00000259818, ENST00000473006, 
ENST00000393193, ENST00000376392, 
ENST00000555572, 
Fusion gene scores* DoF score4 X 4 X 3=487 X 5 X 6=210
# samples 47
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TUBB2B [Title/Abstract] AND NME2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTUBB2B(3227721)-NME2(49244188), # samples:1
Anticipated loss of major functional domain due to fusion event.TUBB2B-NME2 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
TUBB2B-NME2 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
TUBB2B-NME2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
TUBB2B-NME2 seems lost the major protein functional domain in Tgene 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
TgeneNME2

GO:0006165

nucleoside diphosphate phosphorylation

25679041

TgeneNME2

GO:0007229

integrin-mediated signaling pathway

11919189

TgeneNME2

GO:0009142

nucleoside triphosphate biosynthetic process

1851158|25679041

TgeneNME2

GO:0045893

positive regulation of transcription, DNA-templated

8392752

TgeneNME2

GO:0045944

positive regulation of transcription by RNA polymerase II

15703214


check buttonFusion gene breakpoints across TUBB2B (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 NME2 (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
ChimerDB4GBMTCGA-06-5411-01ATUBB2Bchr6

3227721

-NME2chr17

49244188

+


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Fusion Gene ORF analysis for TUBB2B-NME2

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-shiftENST00000259818ENST00000393193TUBB2Bchr6

3227721

-NME2chr17

49244188

+
Frame-shiftENST00000259818ENST00000376392TUBB2Bchr6

3227721

-NME2chr17

49244188

+
Frame-shiftENST00000259818ENST00000555572TUBB2Bchr6

3227721

-NME2chr17

49244188

+
intron-3CDSENST00000473006ENST00000393193TUBB2Bchr6

3227721

-NME2chr17

49244188

+
intron-3CDSENST00000473006ENST00000376392TUBB2Bchr6

3227721

-NME2chr17

49244188

+
intron-3CDSENST00000473006ENST00000555572TUBB2Bchr6

3227721

-NME2chr17

49244188

+

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 TUBB2B-NME2


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)
TUBB2Bchr63227720-NME2chr1749244187+9.85E-060.9999901
TUBB2Bchr63227720-NME2chr1749244187+9.85E-060.9999901

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 TUBB2B-NME2


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
.NME2

O60361

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.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 (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 TUBB2B-NME2


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 TUBB2B-NME2


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 TUBB2B-NME2


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 TUBB2B-NME2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTUBB2BC3552236CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 74CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneTUBB2BC0007097Carcinoma1CTD_human
HgeneTUBB2BC0024667Animal Mammary Neoplasms1CTD_human
HgeneTUBB2BC0024668Mammary Neoplasms, Experimental1CTD_human
HgeneTUBB2BC0205696Anaplastic carcinoma1CTD_human
HgeneTUBB2BC0205697Carcinoma, Spindle-Cell1CTD_human
HgeneTUBB2BC0205698Undifferentiated carcinoma1CTD_human
HgeneTUBB2BC0205699Carcinomatosis1CTD_human
HgeneTUBB2BC0394006Dysequilibrium syndrome1ORPHANET
HgeneTUBB2BC0431380Cortical Dysplasia1CTD_human
HgeneTUBB2BC1257925Mammary Carcinoma, Animal1CTD_human
HgeneTUBB2BC1302995Congenital Fibrosis of the Extraocular Muscles1ORPHANET
HgeneTUBB2BC1955869Malformations of Cortical Development1CTD_human
TgeneNME2C0009402Colorectal Carcinoma1CTD_human
TgeneNME2C0009404Colorectal Neoplasms1CTD_human
TgeneNME2C0019193Hepatitis, Toxic1CTD_human
TgeneNME2C0025500Mesothelioma1CTD_human
TgeneNME2C0029408Degenerative polyarthritis1CTD_human
TgeneNME2C0086743Osteoarthrosis Deformans1CTD_human
TgeneNME2C0860207Drug-Induced Liver Disease1CTD_human
TgeneNME2C0919267ovarian neoplasm1CTD_human
TgeneNME2C1140680Malignant neoplasm of ovary1CTD_human
TgeneNME2C1262760Hepatitis, Drug-Induced1CTD_human
TgeneNME2C3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneNME2C4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneNME2C4279912Chemically-Induced Liver Toxicity1CTD_human