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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:HS3ST5-HDAC2 (FusionGDB2 ID:37450)

Fusion Gene Summary for HS3ST5-HDAC2

check button Fusion gene summary
Fusion gene informationFusion gene name: HS3ST5-HDAC2
Fusion gene ID: 37450
HgeneTgene
Gene symbol

HS3ST5

HDAC2

Gene ID

222537

3066

Gene nameheparan sulfate-glucosamine 3-sulfotransferase 5histone deacetylase 2
Synonyms3-OST-5|3OST5|HS3OST5|NBLA04021HD2|KDAC2|RPD3|YAF1
Cytomap

6q21-q22.1

6q21

Type of geneprotein-codingprotein-coding
Descriptionheparan sulfate glucosamine 3-O-sulfotransferase 5h3-OST-5heparan sulfate (glucosamine) 3-O-sulfotransferase 5heparan sulfate 3-O-sulfotransferase 5heparan sulfate 3-OST-5heparan sulfate D-glucosaminyl 3-O-sulfotransferase 5histone deacetylase 2YY1-associated factor 1transcriptional regulator homolog RPD3
Modification date2020031320200322
UniProtAcc

Q8IZT8

Q92769

Ensembl transtripts involved in fusion geneENST00000312719, ENST00000411826, 
ENST00000441954, 
ENST00000519065, 
ENST00000398283, ENST00000519108, 
ENST00000368632, 
Fusion gene scores* DoF score1 X 1 X 1=16 X 5 X 2=60
# samples 16
** MAII scorelog2(1/1*10)=3.32192809488736log2(6/60*10)=0
Context

PubMed: HS3ST5 [Title/Abstract] AND HDAC2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHS3ST5(114489515)-HDAC2(114281182), # 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
HgeneHS3ST5

GO:0006477

protein sulfation

12138164

HgeneHS3ST5

GO:0015015

heparan sulfate proteoglycan biosynthetic process, enzymatic modification

12138164

HgeneHS3ST5

GO:0046596

regulation of viral entry into host cell

12138164

HgeneHS3ST5

GO:0050819

negative regulation of coagulation

12138164


check buttonFusion gene breakpoints across HS3ST5 (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 HDAC2 (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
ChimerDB4STADTCGA-BR-8365-01AHS3ST5chr6

114489515

-HDAC2chr6

114281182

-


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Fusion Gene ORF analysis for HS3ST5-HDAC2

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
5UTR-3CDSENST00000312719ENST00000519065HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-3CDSENST00000312719ENST00000398283HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-5UTRENST00000312719ENST00000519108HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-5UTRENST00000312719ENST00000368632HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
intron-3CDSENST00000411826ENST00000519065HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
intron-3CDSENST00000411826ENST00000398283HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
intron-5UTRENST00000411826ENST00000519108HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
intron-5UTRENST00000411826ENST00000368632HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-3CDSENST00000441954ENST00000519065HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-3CDSENST00000441954ENST00000398283HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-5UTRENST00000441954ENST00000519108HS3ST5chr6

114489515

-HDAC2chr6

114281182

-
5UTR-5UTRENST00000441954ENST00000368632HS3ST5chr6

114489515

-HDAC2chr6

114281182

-

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 HS3ST5-HDAC2


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 HS3ST5-HDAC2


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
HS3ST5

Q8IZT8

HDAC2

Q92769

FUNCTION: Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) to catalyze the transfer of a sulfo group to position 3 of glucosamine residues in heparan. Catalyzes the rate limiting step in the biosynthesis of heparan sulfate (HSact). This modification is a crucial step in the biosynthesis of anticoagulant heparan sulfate as it completes the structure of the antithrombin pentasaccharide binding site. Also generates GlcUA-GlcNS or IdoUA-GlcNS and IdoUA2S-GlcNH2. The substrate-specific O-sulfation generates an enzyme-modified heparan sulfate which acts as a binding receptor to Herpes simplex virus-1 (HSV-1) and permits its entry. {ECO:0000269|PubMed:12138164}.FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Forms transcriptional repressor complexes by associating with MAD, SIN3, YY1 and N-COR. Interacts in the late S-phase of DNA-replication with DNMT1 in the other transcriptional repressor complex composed of DNMT1, DMAP1, PCNA, CAF1. Deacetylates TSHZ3 and regulates its transcriptional repressor activity. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development. May be involved in the transcriptional repression of circadian target genes, such as PER1, mediated by CRY1 through histone deacetylation. Involved in MTA1-mediated transcriptional corepression of TFF1 and CDKN1A. {ECO:0000269|PubMed:19343227, ECO:0000269|PubMed:21965678}.

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 HS3ST5-HDAC2


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 HS3ST5-HDAC2


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 HS3ST5-HDAC2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHDAC2Q92769DB00175PravastatinInhibitorSmall moleculeApproved
TgeneHDAC2Q92769DB00277TheophyllineActivatorSmall moleculeApproved
TgeneHDAC2Q92769DB00641SimvastatinInhibitorSmall moleculeApproved
TgeneHDAC2Q92769DB01076AtorvastatinInhibitorSmall moleculeApproved
TgeneHDAC2Q92769DB01095FluvastatinInhibitorSmall moleculeApproved
TgeneHDAC2Q92769DB01223AminophyllineActivatorSmall moleculeApproved
TgeneHDAC2Q92769DB01303OxtriphyllineActivatorSmall moleculeApproved
TgeneHDAC2Q92769DB00227LovastatinOtherSmall moleculeApproved|Investigational
TgeneHDAC2Q92769DB00313Valproic acidInhibitorSmall moleculeApproved|Investigational
TgeneHDAC2Q92769DB02546VorinostatInhibitorSmall moleculeApproved|Investigational
TgeneHDAC2Q92769DB06176RomidepsinAntagonist|InhibitorSmall moleculeApproved|Investigational
TgeneHDAC2Q92769DB09091TixocortolStimulatorSmall moleculeApproved|Withdrawn

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Related Diseases for HS3ST5-HDAC2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHS3ST5C0025202melanoma1CTD_human
TgeneHDAC2C0024117Chronic Obstructive Airway Disease2CTD_human
TgeneHDAC2C0525045Mood Disorders2PSYGENET
TgeneHDAC2C1527303Chronic Airflow Obstruction2CTD_human
TgeneHDAC2C0001973Alcoholic Intoxication, Chronic1PSYGENET
TgeneHDAC2C0007137Squamous cell carcinoma1CTD_human
TgeneHDAC2C0011570Mental Depression1PSYGENET
TgeneHDAC2C0014175Endometriosis1CTD_human
TgeneHDAC2C0018800Cardiomegaly1CTD_human
TgeneHDAC2C0023466Leukemia, Monocytic, Chronic1CTD_human
TgeneHDAC2C0023470Myeloid Leukemia1CTD_human
TgeneHDAC2C0023890Liver Cirrhosis1CTD_human
TgeneHDAC2C0025202melanoma1CTD_human
TgeneHDAC2C0033975Psychotic Disorders1PSYGENET
TgeneHDAC2C0036341Schizophrenia1PSYGENET
TgeneHDAC2C0239946Fibrosis, Liver1CTD_human
TgeneHDAC2C0269102Endometrioma1CTD_human
TgeneHDAC2C0349204Nonorganic psychosis1PSYGENET
TgeneHDAC2C0920269Microsatellite Instability1CTD_human
TgeneHDAC2C1383860Cardiac Hypertrophy1CTD_human
TgeneHDAC2C1721098Replication Error Phenotype1CTD_human