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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:HSD17B3-NADSYN1 (FusionGDB2 ID:37675)

Fusion Gene Summary for HSD17B3-NADSYN1

check button Fusion gene summary
Fusion gene informationFusion gene name: HSD17B3-NADSYN1
Fusion gene ID: 37675
HgeneTgene
Gene symbol

HSD17B3

NADSYN1

Gene ID

3293

55191

Gene namehydroxysteroid 17-beta dehydrogenase 3NAD synthetase 1
SynonymsEDH17B3|SDR12C2-
Cytomap

9q22.32

11q13.4

Type of geneprotein-codingprotein-coding
Descriptiontestosterone 17-beta-dehydrogenase 317-beta-HSD 317-beta-HSD317-beta-hydroxysteroid dehydrogenase type 3hydroxysteroid dehydrogenase 3short chain dehydrogenase/reductase family 12C member 2testicular 17-beta-hydroxysteroid dehydrogenaseglutamine-dependent NAD(+) synthetaseNAD(+) synthaseNAD(+) synthetaseglutamine-dependent NAD synthetase
Modification date2020031320200313
UniProtAcc

P37058

Q6IA69

Ensembl transtripts involved in fusion geneENST00000375262, ENST00000375263, 
ENST00000464104, 
ENST00000319023, 
ENST00000526039, ENST00000530055, 
ENST00000539574, 
Fusion gene scores* DoF score4 X 3 X 3=3615 X 16 X 7=1680
# samples 418
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(18/1680*10)=-3.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HSD17B3 [Title/Abstract] AND NADSYN1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHSD17B3(99032156)-NADSYN1(71212586), # 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

check buttonFusion gene breakpoints across HSD17B3 (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 NADSYN1 (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
ChiTaRS5.0N/ABM148284HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-


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Fusion Gene ORF analysis for HSD17B3-NADSYN1

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
intron-3UTRENST00000375262ENST00000319023HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-3UTRENST00000375263ENST00000319023HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-3UTRENST00000464104ENST00000319023HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375262ENST00000526039HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375262ENST00000530055HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375262ENST00000539574HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375263ENST00000526039HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375263ENST00000530055HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000375263ENST00000539574HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000464104ENST00000526039HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000464104ENST00000530055HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-
intron-intronENST00000464104ENST00000539574HSD17B3chr9

99032156

-NADSYN1chr11

71212586

-

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 HSD17B3-NADSYN1


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 HSD17B3-NADSYN1


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/:99032156/:71212586)
- 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
HSD17B3

P37058

NADSYN1

Q6IA69

FUNCTION: Favors the reduction of androstenedione to testosterone. Uses NADPH while the two other EDH17B enzymes use NADH (PubMed:26545797, PubMed:8075637, PubMed:16216911). Androgens such as epiandrosterone, dehydroepiandrosterone, androsterone and androstanedione are accepted as substrates and reduced at C-17. Can reduce 11-ketoandrostenedione as well as 11beta-hydroxyandrostenedione at C-17 to the respective testosterone forms (PubMed:16216911). {ECO:0000269|PubMed:16216911, ECO:0000269|PubMed:26545797, ECO:0000269|PubMed:8075637}.FUNCTION: Catalyzes the final step of the nicotinamide adenine dinucleotide (NAD) de novo synthesis pathway, the ATP-dependent amidation of deamido-NAD using L-glutamine as a nitrogen source. {ECO:0000269|PubMed:12547821, ECO:0000269|PubMed:31883644}.

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 HSD17B3-NADSYN1


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 HSD17B3-NADSYN1


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 HSD17B3-NADSYN1


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 HSD17B3-NADSYN1


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