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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:TOM1L2-NXN

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TOM1L2-NXN
FusionPDB ID: 93002
FusionGDB2.0 ID: 93002
HgeneTgene
Gene symbol

TOM1L2

NXN

Gene ID

146691

64359

Gene nametarget of myb1 like 2 membrane trafficking proteinnucleoredoxin
Synonyms-NRX|RRS2|TRG-4
Cytomap

17p11.2

17p13.3

Type of geneprotein-codingprotein-coding
DescriptionTOM1-like protein 2target of Myb-like protein 2target of myb1-like 2nucleoredoxinnucleoredoxin 1
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000379504, ENST00000535933, 
ENST00000581396, ENST00000318094, 
ENST00000395739, ENST00000478943, 
ENST00000540946, ENST00000542206, 
ENST00000577517, 
ENST00000537628, 
ENST00000575801, ENST00000577098, 
ENST00000538650, ENST00000336868, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 13 X 7=145617 X 15 X 5=1275
# samples 1720
** MAII scorelog2(17/1456*10)=-3.098403704061
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/1275*10)=-2.6724253419715
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: TOM1L2 [Title/Abstract] AND NXN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TOM1L2(17787948)-NXN(729318), # samples:2
Anticipated loss of major functional domain due to fusion event.TOM1L2-NXN seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
TOM1L2-NXN seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
TOM1L2-NXN seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
TOM1L2-NXN seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneTOM1L2

GO:0007165

signal transduction

16479011

HgeneTOM1L2

GO:0045839

negative regulation of mitotic nuclear division

16479011


check buttonFusion gene breakpoints across TOM1L2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4STADTCGA-CG-4477-01ATOM1L2chr17

17787948

-NXNchr17

729318

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000581396TOM1L2chr1717787948-ENST00000336868NXNchr17729318-3032448971395432
ENST00000379504TOM1L2chr1717787948-ENST00000336868NXNchr17729318-3169585841532482
ENST00000535933TOM1L2chr1717787948-ENST00000336868NXNchr17729318-31926081071555482

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
ENST00000581396ENST00000336868TOM1L2chr1717787948-NXNchr17729318-0.0040481440.9959519
ENST00000379504ENST00000336868TOM1L2chr1717787948-NXNchr17729318-0.0034739690.99652606
ENST00000535933ENST00000336868TOM1L2chr1717787948-NXNchr17729318-0.0034108640.9965892

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>93002_93002_1_TOM1L2-NXN_TOM1L2_chr17_17787948_ENST00000379504_NXN_chr17_729318_ENST00000336868_length(amino acids)=482AA_BP=167
MEFLLGNPFSTPVGQCLEKATDGSLQSEDWTLNMEICDIINETEEGPKDAIRALKKRLNGNRNYREVMLALTVLETCVKNCGHRFHILVA
NRDFIDSVLVKIISPKNNPPTIVQDKVLALIQAWADAFRSSPDLTGVVHIYEELKRKGVEFPMADLDALSPIHTPQRLKLWNKYRISNIP
SLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIK
EAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVL
ELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLFFVAGEDDMTDSLRDYTNLPEAAPLLTILDMSAR

--------------------------------------------------------------

>93002_93002_2_TOM1L2-NXN_TOM1L2_chr17_17787948_ENST00000535933_NXN_chr17_729318_ENST00000336868_length(amino acids)=482AA_BP=167
MEFLLGNPFSTPVGQCLEKATDGSLQSEDWTLNMEICDIINETEEGPKDAIRALKKRLNGNRNYREVMLALTVLETCVKNCGHRFHILVA
NRDFIDSVLVKIISPKNNPPTIVQDKVLALIQAWADAFRSSPDLTGVVHIYEELKRKGVEFPMADLDALSPIHTPQRLKLWNKYRISNIP
SLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIK
EAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVL
ELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLFFVAGEDDMTDSLRDYTNLPEAAPLLTILDMSAR

--------------------------------------------------------------

>93002_93002_3_TOM1L2-NXN_TOM1L2_chr17_17787948_ENST00000581396_NXN_chr17_729318_ENST00000336868_length(amino acids)=432AA_BP=117
MEFLLGNPFSTPVGQCLEKATDGSLQSEDWTLNMEICDIINETEEGPKDAIRALKKRLNGNRNYREVMLALTAWADAFRSSPDLTGVVHI
YEELKRKGVEFPMADLDALSPIHTPQRLKLWNKYRISNIPSLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNG
QSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQ
GIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKE

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Fusion Protein Functional Features


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/chr17:17787948/chr17:729318)
- 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
..
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: 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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTOM1L2chr17:17787948chr17:729318ENST00000379504-51520_152167.0508.0DomainVHS
TgeneNXNchr17:17787948chr17:729318ENST0000033686808167_321120.0436.0DomainThioredoxin
TgeneNXNchr17:17787948chr17:729318ENST0000053762808167_3210187.0DomainThioredoxin
TgeneNXNchr17:17787948chr17:729318ENST0000057580108167_32112.0328.0DomainThioredoxin

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTOM1L2chr17:17787948chr17:729318ENST00000318094-11420_1520463.0DomainVHS
HgeneTOM1L2chr17:17787948chr17:729318ENST00000318094-114219_3070463.0DomainGAT
HgeneTOM1L2chr17:17787948chr17:729318ENST00000379504-515219_307167.0508.0DomainGAT
HgeneTOM1L2chr17:17787948chr17:729318ENST00000395739-11420_1520463.0DomainVHS
HgeneTOM1L2chr17:17787948chr17:729318ENST00000395739-114219_3070463.0DomainGAT
HgeneTOM1L2chr17:17787948chr17:729318ENST00000478943-1920_1520241.0DomainVHS
HgeneTOM1L2chr17:17787948chr17:729318ENST00000478943-19219_3070241.0DomainGAT
HgeneTOM1L2chr17:17787948chr17:729318ENST00000581396-41420_152117.0458.0DomainVHS
HgeneTOM1L2chr17:17787948chr17:729318ENST00000581396-414219_307117.0458.0DomainGAT
HgeneTOM1L2chr17:17787948chr17:729318ENST00000318094-114329_3340463.0MotifNote=Clathrin-binding
HgeneTOM1L2chr17:17787948chr17:729318ENST00000379504-515329_334167.0508.0MotifNote=Clathrin-binding
HgeneTOM1L2chr17:17787948chr17:729318ENST00000395739-114329_3340463.0MotifNote=Clathrin-binding
HgeneTOM1L2chr17:17787948chr17:729318ENST00000478943-19329_3340241.0MotifNote=Clathrin-binding
HgeneTOM1L2chr17:17787948chr17:729318ENST00000581396-414329_334117.0458.0MotifNote=Clathrin-binding


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
TOM1L2
NXN


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to TOM1L2-NXN


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to TOM1L2-NXN


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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