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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:SLX4-ADAM32

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SLX4-ADAM32
FusionPDB ID: 83742
FusionGDB2.0 ID: 83742
HgeneTgene
Gene symbol

SLX4

ADAM32

Gene ID

84464

203102

Gene nameSLX4 structure-specific endonuclease subunitADAM metallopeptidase domain 32
SynonymsBTBD12|FANCP|MUS312-
Cytomap

16p13.3

8p11.22

Type of geneprotein-codingprotein-coding
Descriptionstructure-specific endonuclease subunit SLX4BTB/POZ domain-containing protein 12disintegrin and metalloproteinase domain-containing protein 32a disintegrin and metalloprotease domain 32a disintegrin and metalloproteinase domain 32metalloproteinase 12-like proteintesticular tissue protein Li 13
Modification date2020032720200313
UniProtAcc

Q5VYV7

Q8TC27

Ensembl transtripts involved in fusion geneENST idsENST00000294008, ENST00000524303, 
ENST00000379907, ENST00000437682, 
ENST00000519315, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 3=4811 X 12 X 8=1056
# samples 413
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/1056*10)=-3.02202630633
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SLX4 [Title/Abstract] AND ADAM32 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SLX4(3650980)-ADAM32(39114706), # samples:2
Anticipated loss of major functional domain due to fusion event.SLX4-ADAM32 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.
SLX4-ADAM32 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.
SLX4-ADAM32 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.
SLX4-ADAM32 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

check buttonFusion gene breakpoints across SLX4 (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 ADAM32 (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
ChimerDB4BRCATCGA-C8-A8HP-01ASLX4chr16

3650980

-ADAM32chr8

39114706

+


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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)
ENST00000294008SLX4chr163650980-ENST00000437682ADAM32chr839114706+227318046411837398
ENST00000294008SLX4chr163650980-ENST00000519315ADAM32chr839114706+211718046411837398
ENST00000294008SLX4chr163650980-ENST00000379907ADAM32chr839114706+227318046411837398

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
ENST00000294008ENST00000437682SLX4chr163650980-ADAM32chr839114706+0.0110667220.9889333
ENST00000294008ENST00000519315SLX4chr163650980-ADAM32chr839114706+0.0059680460.99403197
ENST00000294008ENST00000379907SLX4chr163650980-ADAM32chr839114706+0.0110667220.9889333

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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

>83742_83742_1_SLX4-ADAM32_SLX4_chr16_3650980_ENST00000294008_ADAM32_chr8_39114706_ENST00000379907_length(amino acids)=398AA_BP=
MKLSVNEAQLGFYLGSLSHLSACPGIDPRSSEDQPESLKTGQMMDESDEDFKELCASFFQRVKKHGIKEVSGERKTQKAASNGTQIRSKL
KRTKQTATKTKTLQGPAEKKPPSGSQAPRTKKQRVTKWQASEPAHSVNGEGGVLASAPDPPVLRETAQNTQTGNQQEPSPNLSREKTREN
VPNSDSQPPPSCLTTAVPSPSKPRTAQLVLQRMQQFKRADPERLRHASEECSLEAAREENVPKDPQEEMMAGNVYGLGPPAPESDAAVAL
TLQQEFARVGASAHDDSLEEKGLFFCQICQKNLSAMNVTRREQHVNRCLDEAEKTLRPSVPQIPECPICGKPFLTLKSRTSHLKQCAVKM

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

>83742_83742_2_SLX4-ADAM32_SLX4_chr16_3650980_ENST00000294008_ADAM32_chr8_39114706_ENST00000437682_length(amino acids)=398AA_BP=
MKLSVNEAQLGFYLGSLSHLSACPGIDPRSSEDQPESLKTGQMMDESDEDFKELCASFFQRVKKHGIKEVSGERKTQKAASNGTQIRSKL
KRTKQTATKTKTLQGPAEKKPPSGSQAPRTKKQRVTKWQASEPAHSVNGEGGVLASAPDPPVLRETAQNTQTGNQQEPSPNLSREKTREN
VPNSDSQPPPSCLTTAVPSPSKPRTAQLVLQRMQQFKRADPERLRHASEECSLEAAREENVPKDPQEEMMAGNVYGLGPPAPESDAAVAL
TLQQEFARVGASAHDDSLEEKGLFFCQICQKNLSAMNVTRREQHVNRCLDEAEKTLRPSVPQIPECPICGKPFLTLKSRTSHLKQCAVKM

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

>83742_83742_3_SLX4-ADAM32_SLX4_chr16_3650980_ENST00000294008_ADAM32_chr8_39114706_ENST00000519315_length(amino acids)=398AA_BP=
MKLSVNEAQLGFYLGSLSHLSACPGIDPRSSEDQPESLKTGQMMDESDEDFKELCASFFQRVKKHGIKEVSGERKTQKAASNGTQIRSKL
KRTKQTATKTKTLQGPAEKKPPSGSQAPRTKKQRVTKWQASEPAHSVNGEGGVLASAPDPPVLRETAQNTQTGNQQEPSPNLSREKTREN
VPNSDSQPPPSCLTTAVPSPSKPRTAQLVLQRMQQFKRADPERLRHASEECSLEAAREENVPKDPQEEMMAGNVYGLGPPAPESDAAVAL
TLQQEFARVGASAHDDSLEEKGLFFCQICQKNLSAMNVTRREQHVNRCLDEAEKTLRPSVPQIPECPICGKPFLTLKSRTSHLKQCAVKM

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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/chr16:3650980/chr8:39114706)
- 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
SLX4

Q5VYV7

ADAM32

Q8TC27

FUNCTION: May play a role in sperm development and fertilization This is a non-catalytic metalloprotease-like protein. {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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515293_323387.66666666666671835.0Zinc fingerUBZ4-type 1
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515333_361387.66666666666671835.0Zinc fingerUBZ4-type 2
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725704_787668.3333333333334788.0Topological domainCytoplasmic
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725683_703668.3333333333334788.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515801_870387.66666666666671835.0Coiled coilOntology_term=ECO:0000255
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-5151710_1721387.66666666666671835.0Compositional biasNote=Poly-Ser
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515520_523387.66666666666671835.0Compositional biasNote=Poly-Pro
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515796_856387.66666666666671835.0Compositional biasNote=Glu-rich
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515691_764387.66666666666671835.0DomainBTB
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725480_502668.3333333333334788.0Compositional biasNote=Cys-rich
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725186_383668.3333333333334788.0DomainPeptidase M12B
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725391_479668.3333333333334788.0DomainDisintegrin
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725622_654668.3333333333334788.0DomainEGF-like
TgeneADAM32chr16:3650980chr8:39114706ENST000003799071725175_682668.3333333333334788.0Topological domainExtracellular


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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
SLX4
ADAM32


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
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-5151328_1648387.66666666666671835.0MUS81
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-515684_1834387.66666666666671835.0PLK1 and TERF2-TERF2IP
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-5151632_1834387.66666666666671835.0SLX1
HgeneSLX4chr16:3650980chr8:39114706ENST00000294008-5151_669387.66666666666671835.0SLX4IP%2C ERCC4/XPF and MSH2


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Related Drugs to SLX4-ADAM32


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 SLX4-ADAM32


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