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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:ATP5J-HCN1 (FusionGDB2 ID:8092)

Fusion Gene Summary for ATP5J-HCN1

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP5J-HCN1
Fusion gene ID: 8092
HgeneTgene
Gene symbol

ATP5J

HCN1

Gene ID

522

348980

Gene nameATP synthase peripheral stalk subunit F6hyperpolarization activated cyclic nucleotide gated potassium channel 1
SynonymsATP5|ATP5A|ATP5J|ATPM|CF6|F6BCNG-1|BCNG1|EIEE24|GEFSP10|HAC-2
Cytomap

21q21.3

5p12

Type of geneprotein-codingprotein-coding
DescriptionATP synthase-coupling factor 6, mitochondrialATP synthase, H+ transporting, mitochondrial F0 complex, subunit F6ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6ATPase subunit F6coupling factor 6mitochondrial ATP synthase, coupling fpotassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1brain cyclic nucleotide-gated channel 1
Modification date2020031320200313
UniProtAcc.

O60741

Ensembl transtripts involved in fusion geneENST00000400099, ENST00000400094, 
ENST00000284971, ENST00000457143, 
ENST00000400090, ENST00000400087, 
ENST00000400093, 
ENST00000303230, 
Fusion gene scores* DoF score10 X 11 X 4=4407 X 6 X 6=252
# samples 118
** MAII scorelog2(11/440*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/252*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATP5J [Title/Abstract] AND HCN1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATP5J(27107164)-HCN1(45462109), # samples:2
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
HgeneATP5J

GO:0042776

mitochondrial ATP synthesis coupled proton transport

12110673

TgeneHCN1

GO:0051289

protein homotetramerization

28086084

TgeneHCN1

GO:0071320

cellular response to cAMP

22748890


check buttonFusion gene breakpoints across ATP5J (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 HCN1 (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
ChimerDB4KIRPTCGA-B9-A5W9-01AATP5Jchr21

27107164

-HCN1chr5

45462109

-
ChimerDB4KIRPTCGA-B9-A5W9ATP5Jchr21

27107163

-HCN1chr5

45462109

-
ChimerDB4KIRPTCGA-B9-A5W9ATP5Jchr21

27107164

-HCN1chr5

45462109

-


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Fusion Gene ORF analysis for ATP5J-HCN1

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-3CDSENST00000400099ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
5UTR-3CDSENST00000400094ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
5UTR-3CDSENST00000284971ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
intron-3CDSENST00000457143ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
intron-3CDSENST00000400090ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
intron-3CDSENST00000400087ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
intron-3CDSENST00000400093ENST00000303230ATP5Jchr21

27107164

-HCN1chr5

45462109

-
intron-3CDSENST00000400099ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
5UTR-3CDSENST00000400094ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
5UTR-3CDSENST00000284971ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
intron-3CDSENST00000457143ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
intron-3CDSENST00000400090ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
intron-3CDSENST00000400087ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-
intron-3CDSENST00000400093ENST00000303230ATP5Jchr21

27107163

-HCN1chr5

45462109

-

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 ATP5J-HCN1


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 ATP5J-HCN1


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
.HCN1

O60741

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: Hyperpolarization-activated ion channel exhibiting weak selectivity for potassium over sodium ions (PubMed:28086084). Contributes to the native pacemaker currents in heart (If) and in neurons (Ih). May mediate responses to sour stimuli. {ECO:0000269|PubMed:15351778, ECO:0000269|PubMed:28086084, ECO:0000269|PubMed:29936235, ECO:0000269|PubMed:30351409}.

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 ATP5J-HCN1


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 ATP5J-HCN1


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 ATP5J-HCN1


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 ATP5J-HCN1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneHCN1C4014531EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 243CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneHCN1C0011581Depressive disorder2PSYGENET
TgeneHCN1C0004134Ataxia1CTD_human
TgeneHCN1C0011570Mental Depression1PSYGENET
TgeneHCN1C0014544Epilepsy1CTD_human
TgeneHCN1C0022333Jacksonian Seizure1CTD_human
TgeneHCN1C0036572Seizures1CTD_human
TgeneHCN1C0086237Epilepsy, Cryptogenic1CTD_human
TgeneHCN1C0149958Complex partial seizures1CTD_human
TgeneHCN1C0234533Generalized seizures1CTD_human
TgeneHCN1C0234535Clonic Seizures1CTD_human
TgeneHCN1C0236018Aura1CTD_human
TgeneHCN1C0240991Ataxia, Sensory1CTD_human
TgeneHCN1C0270824Visual seizure1CTD_human
TgeneHCN1C0270844Tonic Seizures1CTD_human
TgeneHCN1C0270846Epileptic drop attack1CTD_human
TgeneHCN1C0278161Ataxia, Motor1CTD_human
TgeneHCN1C0422850Seizures, Somatosensory1CTD_human
TgeneHCN1C0422852Seizures, Auditory1CTD_human
TgeneHCN1C0422853Olfactory seizure1CTD_human
TgeneHCN1C0422854Gustatory seizure1CTD_human
TgeneHCN1C0422855Vertiginous seizure1CTD_human
TgeneHCN1C0427190Ataxia, Truncal1CTD_human
TgeneHCN1C0494475Tonic - clonic seizures1CTD_human
TgeneHCN1C0520966Abnormal coordination1CTD_human
TgeneHCN1C0750937Ataxia, Appendicular1CTD_human
TgeneHCN1C0750940Tremor, Rubral1CTD_human
TgeneHCN1C0751056Non-epileptic convulsion1CTD_human
TgeneHCN1C0751110Single Seizure1CTD_human
TgeneHCN1C0751111Awakening Epilepsy1CTD_human
TgeneHCN1C0751123Atonic Absence Seizures1CTD_human
TgeneHCN1C0751494Convulsive Seizures1CTD_human
TgeneHCN1C0751495Seizures, Focal1CTD_human
TgeneHCN1C0751496Seizures, Sensory1CTD_human
TgeneHCN1C3463992EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11CTD_human
TgeneHCN1C3495874Nonepileptic Seizures1CTD_human
TgeneHCN1C3502809Generalized Epilepsy with Febrile Seizures Plus1ORPHANET
TgeneHCN1C4048158Convulsions1CTD_human
TgeneHCN1C4316903Absence Seizures1CTD_human
TgeneHCN1C4317109Epileptic Seizures1CTD_human
TgeneHCN1C4317123Myoclonic Seizures1CTD_human
TgeneHCN1C4505436Generalized Absence Seizures1CTD_human
TgeneHCN1C4552072X-linked infantile spasms1CTD_human