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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:PER2-HDAC4 (FusionGDB2 ID:63896)

Fusion Gene Summary for PER2-HDAC4

check button Fusion gene summary
Fusion gene informationFusion gene name: PER2-HDAC4
Fusion gene ID: 63896
HgeneTgene
Gene symbol

PER2

HDAC4

Gene ID

8864

9759

Gene nameperiod circadian regulator 2histone deacetylase 4
SynonymsFASPS|FASPS1AHO3|BDMR|HA6116|HD4|HDAC-4|HDAC-A|HDACA
Cytomap

2q37.3

2q37.3

Type of geneprotein-codingprotein-coding
Descriptionperiod circadian protein homolog 2circadian clock protein PERIOD 2hPER2period 2period circadian clock 2period circadian protein 2period homolog 2histone deacetylase 4histone deacetylase A
Modification date2020032220200329
UniProtAcc.

P56524

Ensembl transtripts involved in fusion geneENST00000254658, ENST00000254657, 
ENST00000440245, ENST00000355768, 
ENST00000345617, ENST00000543185, 
ENST00000541256, ENST00000553145, 
Fusion gene scores* DoF score3 X 3 X 3=2711 X 11 X 4=484
# samples 311
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/484*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PER2 [Title/Abstract] AND HDAC4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHDAC4(239583758)-PER2(239182157), # samples:1
PER2(239157703)-HDAC4(240037006), # samples:1
Anticipated loss of major functional domain due to fusion event.PER2-HDAC4 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
PER2-HDAC4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PER2-HDAC4 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PER2-HDAC4 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor 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
TgeneHDAC4

GO:0000122

negative regulation of transcription by RNA polymerase II

10869435|16236793

TgeneHDAC4

GO:0006338

chromatin remodeling

18850004

TgeneHDAC4

GO:0006476

protein deacetylation

27708256

TgeneHDAC4

GO:0016575

histone deacetylation

10869435

TgeneHDAC4

GO:0033235

positive regulation of protein sumoylation

17696781

TgeneHDAC4

GO:0034983

peptidyl-lysine deacetylation

18614528

TgeneHDAC4

GO:0045892

negative regulation of transcription, DNA-templated

10869435

TgeneHDAC4

GO:0070932

histone H3 deacetylation

12590135

TgeneHDAC4

GO:0070933

histone H4 deacetylation

12590135


check buttonFusion gene breakpoints across PER2 (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 HDAC4 (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
ChimerDB4SKCMTCGA-D3-A3MO-06APER2chr2

239157703

-HDAC4chr2

240037006

-


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Fusion Gene ORF analysis for PER2-HDAC4

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
3UTR-3CDSENST00000254658ENST00000345617PER2chr2

239157703

-HDAC4chr2

240037006

-
3UTR-3CDSENST00000254658ENST00000543185PER2chr2

239157703

-HDAC4chr2

240037006

-
3UTR-3CDSENST00000254658ENST00000541256PER2chr2

239157703

-HDAC4chr2

240037006

-
3UTR-intronENST00000254658ENST00000553145PER2chr2

239157703

-HDAC4chr2

240037006

-
Frame-shiftENST00000254657ENST00000345617PER2chr2

239157703

-HDAC4chr2

240037006

-
Frame-shiftENST00000254657ENST00000543185PER2chr2

239157703

-HDAC4chr2

240037006

-
Frame-shiftENST00000254657ENST00000541256PER2chr2

239157703

-HDAC4chr2

240037006

-
5CDS-intronENST00000254657ENST00000553145PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000440245ENST00000345617PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000440245ENST00000543185PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000440245ENST00000541256PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-intronENST00000440245ENST00000553145PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000355768ENST00000345617PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000355768ENST00000543185PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-3CDSENST00000355768ENST00000541256PER2chr2

239157703

-HDAC4chr2

240037006

-
intron-intronENST00000355768ENST00000553145PER2chr2

239157703

-HDAC4chr2

240037006

-

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 PER2-HDAC4


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 PER2-HDAC4


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
.HDAC4

P56524

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: 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. Involved in muscle maturation via its interaction with the myocyte enhancer factors such as MEF2A, MEF2C and MEF2D. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Deacetylates HSPA1A and HSPA1B at 'Lys-77' leading to their preferential binding to co-chaperone STUB1 (PubMed:27708256). {ECO:0000269|PubMed:10523670, ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:27708256}.

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 PER2-HDAC4


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 PER2-HDAC4


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 PER2-HDAC4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHDAC4P56524DB14548Zinc sulfate, unspecified formCofactorSmall moleculeApproved|Experimental
TgeneHDAC4P56524DB14548Zinc sulfate, unspecified formCofactorSmall moleculeApproved|Experimental
TgeneHDAC4P56524DB01593ZincCofactorSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB01593ZincCofactorSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB06176RomidepsinInhibitorSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB06176RomidepsinInhibitorSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB14487Zinc acetateSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB14487Zinc acetateSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB14533Zinc chlorideCofactorSmall moleculeApproved|Investigational
TgeneHDAC4P56524DB14533Zinc chlorideCofactorSmall moleculeApproved|Investigational

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Related Diseases for PER2-HDAC4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePER2C0011570Mental Depression5PSYGENET
HgenePER2C0011581Depressive disorder5PSYGENET
HgenePER2C0005586Bipolar Disorder4PSYGENET
HgenePER2C0038587Substance Withdrawal Syndrome2CTD_human
HgenePER2C0086189Drug Withdrawal Symptoms2CTD_human
HgenePER2C0087169Withdrawal Symptoms2CTD_human
HgenePER2C0221074Depression, Postpartum2PSYGENET
HgenePER2C0600427Cocaine Dependence2PSYGENET
HgenePER2C0001969Alcoholic Intoxication1CTD_human
HgenePER2C0023473Myeloid Leukemia, Chronic1CTD_human
HgenePER2C0858355Addicted to cocaine1PSYGENET
HgenePER2C1858496Advanced Sleep-Phase Syndrome, Familial1CTD_human;ORPHANET
HgenePER2C3807327ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 11GENOMICS_ENGLAND;UNIPROT
TgeneHDAC4C2931817Chromosome 2q37 deletion syndrome4CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneHDAC4C0036341Schizophrenia2PSYGENET
TgeneHDAC4C0005684Malignant neoplasm of urinary bladder1CTD_human
TgeneHDAC4C0005695Bladder Neoplasm1CTD_human
TgeneHDAC4C0009171Cocaine Abuse1CTD_human
TgeneHDAC4C0011570Mental Depression1PSYGENET
TgeneHDAC4C0011616Contact Dermatitis1CTD_human
TgeneHDAC4C0020796Profound Mental Retardation1CTD_human
TgeneHDAC4C0025363Mental Retardation, Psychosocial1CTD_human
TgeneHDAC4C0162351Contact hypersensitivity1CTD_human
TgeneHDAC4C0221357Brachydactyly1CTD_human
TgeneHDAC4C0236736Cocaine-Related Disorders1CTD_human
TgeneHDAC4C0340543Familial primary pulmonary hypertension1CTD_human
TgeneHDAC4C0345967Malignant mesothelioma1CTD_human
TgeneHDAC4C0525045Mood Disorders1PSYGENET
TgeneHDAC4C0600427Cocaine Dependence1CTD_human
TgeneHDAC4C0917816Mental deficiency1CTD_human
TgeneHDAC4C1862102BRACHYDACTYLY, TYPE E11CTD_human
TgeneHDAC4C1969342PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED1CTD_human
TgeneHDAC4C1969343Pulmonary Hypertension, Primary, Fenfluramine-Associated1CTD_human
TgeneHDAC4C3203102Idiopathic pulmonary arterial hypertension1CTD_human
TgeneHDAC4C3714756Intellectual Disability1CTD_human
TgeneHDAC4C3714844Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia1CTD_human
TgeneHDAC4C4552070Pulmonary Hypertension, Primary, 11CTD_human