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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:ABCB8-NOS3 (FusionGDB2 ID:220)

Fusion Gene Summary for ABCB8-NOS3

check button Fusion gene summary
Fusion gene informationFusion gene name: ABCB8-NOS3
Fusion gene ID: 220
HgeneTgene
Gene symbol

ABCB8

NOS3

Gene ID

11194

342977

Gene nameATP binding cassette subfamily B member 8nanos C2HC-type zinc finger 3
SynonymsEST328128|M-ABC1|MABC1|MITOSURNANOS1L|NOS3|ZC2HC12C
Cytomap

7q36.1

19p13.12

Type of geneprotein-codingprotein-coding
Descriptionmitochondrial potassium channel ATP-binding subunitATP-binding cassette sub-family B member 8, mitochondrialATP-binding cassette, sub-family B (MDR/TAP), member 8mitochondrial ABC proteinmitochondrial ATP-binding cassette 1mitochondrial sulfonylurea-nanos homolog 3
Modification date2020031320200313
UniProtAcc

Q9NUT2

.
Ensembl transtripts involved in fusion geneENST00000297504, ENST00000356058, 
ENST00000358849, ENST00000477092, 
ENST00000477719, ENST00000498578, 
ENST00000542328, ENST00000493338, 
ENST00000467517, ENST00000477227, 
ENST00000484524, ENST00000297494, 
ENST00000461406, 
Fusion gene scores* DoF score4 X 4 X 5=804 X 5 X 4=80
# samples 55
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ABCB8 [Title/Abstract] AND NOS3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointABCB8(150725697)-NOS3(150706018), # samples:6
Anticipated loss of major functional domain due to fusion event.ABCB8-NOS3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ABCB8-NOS3 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ABCB8-NOS3 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneABCB8

GO:0071805

potassium ion transmembrane transport

31435016

TgeneNOS3

GO:0017148

negative regulation of translation

24736845

TgeneNOS3

GO:1900153

positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay

24736845


check buttonFusion gene breakpoints across ABCB8 (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 NOS3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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-AC-A3TN-01AABCB8chr7

150725697

-NOS3chr7

150706018

+
ChimerDB4BRCATCGA-AC-A3TN-01AABCB8chr7

150725697

+NOS3chr7

150706018

+
ChimerDB4LUADTCGA-MP-A4TA-01AABCB8chr7

150725696

+NOS3chr7

150706017

+
ChimerDB4LUADTCGA-MP-A4TA-01AABCB8chr7

150725697

-NOS3chr7

150706018

+
ChimerDB4LUADTCGA-MP-A4TA-01AABCB8chr7

150725697

+NOS3chr7

150706018

+


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Fusion Gene ORF analysis for ABCB8-NOS3

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
5CDS-intronENST00000297504ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000297504ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000297504ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000297504ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000297504ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000297504ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000356058ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000356058ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000356058ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000356058ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000356058ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000356058ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000358849ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000358849ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000358849ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000358849ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000358849ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000358849ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477092ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477092ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477092ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477092ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477092ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477092ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477719ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477719ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477719ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477719ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000477719ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000477719ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000498578ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000498578ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000498578ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000498578ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000498578ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000498578ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000542328ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000542328ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000542328ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000542328ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
5CDS-intronENST00000542328ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
5CDS-intronENST00000542328ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000297504ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000297504ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000297504ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000297504ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000356058ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000356058ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000356058ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000356058ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000358849ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000358849ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000358849ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000358849ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000477092ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000477092ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000477092ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000477092ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000477719ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000477719ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000477719ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000477719ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000498578ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000498578ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
Frame-shiftENST00000498578ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
Frame-shiftENST00000498578ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
In-frameENST00000542328ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
In-frameENST00000542328ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
In-frameENST00000542328ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
In-frameENST00000542328ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
intron-3CDSENST00000493338ENST00000297494ABCB8chr7

150725697

+NOS3chr7

150706018

+
intron-3CDSENST00000493338ENST00000297494ABCB8chr7

150725696

+NOS3chr7

150706017

+
intron-3CDSENST00000493338ENST00000461406ABCB8chr7

150725697

+NOS3chr7

150706018

+
intron-3CDSENST00000493338ENST00000461406ABCB8chr7

150725696

+NOS3chr7

150706017

+
intron-intronENST00000493338ENST00000467517ABCB8chr7

150725697

+NOS3chr7

150706018

+
intron-intronENST00000493338ENST00000467517ABCB8chr7

150725696

+NOS3chr7

150706017

+
intron-intronENST00000493338ENST00000477227ABCB8chr7

150725697

+NOS3chr7

150706018

+
intron-intronENST00000493338ENST00000477227ABCB8chr7

150725696

+NOS3chr7

150706017

+
intron-intronENST00000493338ENST00000484524ABCB8chr7

150725697

+NOS3chr7

150706018

+
intron-intronENST00000493338ENST00000484524ABCB8chr7

150725696

+NOS3chr7

150706017

+

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 ABCB8-NOS3


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)
ABCB8chr7150725697+NOS3chr7150706017+0.0475845860.9524154
ABCB8chr7150725697+NOS3chr7150706017+0.0475845860.9524154

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.
genomic feature

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.
genomic feature of top 1%

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Fusion Protein Features for ABCB8-NOS3


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/chr7:150725697/chr7:150706018)
- 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
ABCB8

Q9NUT2

.
FUNCTION: ATP-binding subunit of the mitochondrial potassium channel located in the mitochondrial inner membrane (PubMed:31435016). Together with CCDC51/MITOK, forms a protein complex localized in the mitochondria that mediates ATP-dependent potassium currents across the inner membrane (that is, mitoK(ATP) channel) (PubMed:31435016). Plays a role in mitochondrial iron transport (PubMed:30623799). Required for maintenance of normal cardiac function, possibly by influencing mitochondrial iron export and regulating the maturation of cytosolic iron sulfur cluster-containing enzymes (By similarity). {ECO:0000250|UniProtKB:Q9CXJ4, ECO:0000269|PubMed:30623799, ECO:0000269|PubMed:31435016}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627756_10027041204.0DomainFAD-binding FR-type
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014520_7030630.0DomainFlavodoxin-like
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014756_10020630.0DomainFAD-binding FR-type
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627756_10027041204.0DomainFAD-binding FR-type
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014520_7030630.0DomainFlavodoxin-like
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014756_10020630.0DomainFAD-binding FR-type
TgeneNOS3chr7:150725696chr7:150706017ENST0000029749416271010_10287041204.0Nucleotide bindingNADP
TgeneNOS3chr7:150725696chr7:150706017ENST0000029749416271108_11237041204.0Nucleotide bindingNADP
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627793_8047041204.0Nucleotide bindingFAD
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627935_9457041204.0Nucleotide bindingFAD
TgeneNOS3chr7:150725696chr7:150706017ENST000004845240141010_10280630.0Nucleotide bindingNADP
TgeneNOS3chr7:150725696chr7:150706017ENST000004845240141108_11230630.0Nucleotide bindingNADP
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014649_6800630.0Nucleotide bindingFMN
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014793_8040630.0Nucleotide bindingFAD
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014935_9450630.0Nucleotide bindingFAD
TgeneNOS3chr7:150725697chr7:150706018ENST0000029749416271010_10287041204.0Nucleotide bindingNADP
TgeneNOS3chr7:150725697chr7:150706018ENST0000029749416271108_11237041204.0Nucleotide bindingNADP
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627793_8047041204.0Nucleotide bindingFAD
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627935_9457041204.0Nucleotide bindingFAD
TgeneNOS3chr7:150725697chr7:150706018ENST000004845240141010_10280630.0Nucleotide bindingNADP
TgeneNOS3chr7:150725697chr7:150706018ENST000004845240141108_11230630.0Nucleotide bindingNADP
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014649_6800630.0Nucleotide bindingFMN
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014793_8040630.0Nucleotide bindingFAD
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014935_9450630.0Nucleotide bindingFAD
TgeneNOS3chr7:150725696chr7:150706017ENST00000484524014491_5100630.0RegionCalmodulin-binding
TgeneNOS3chr7:150725697chr7:150706018ENST00000484524014491_5100630.0RegionCalmodulin-binding

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117150_43731736.0DomainABC transmembrane type-1
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117472_70931736.0DomainABC transporter
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116150_43731719.0DomainABC transmembrane type-1
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116472_70931719.0DomainABC transporter
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117150_43731736.0DomainABC transmembrane type-1
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117472_70931736.0DomainABC transporter
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116150_43731719.0DomainABC transmembrane type-1
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116472_70931719.0DomainABC transporter
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117507_51431736.0Nucleotide bindingATP
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116507_51431719.0Nucleotide bindingATP
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117507_51431736.0Nucleotide bindingATP
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116507_51431719.0Nucleotide bindingATP
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117166_19531736.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117217_29531736.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+11726_14431736.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117317_73531736.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116166_19531719.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116217_29531719.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+11626_14431719.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116317_73531719.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117166_19531736.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117217_29531736.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+11726_14431736.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117317_73531736.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116166_19531719.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116217_29531719.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+11626_14431719.0Topological domainMitochondrial matrix
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116317_73531719.0Topological domainMitochondrial intermembrane
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117145_16531736.0TransmembraneHelical
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117196_21631736.0TransmembraneHelical
HgeneABCB8chr7:150725696chr7:150706017ENST00000297504+117296_31631736.0TransmembraneHelical
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116145_16531719.0TransmembraneHelical
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116196_21631719.0TransmembraneHelical
HgeneABCB8chr7:150725696chr7:150706017ENST00000358849+116296_31631719.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117145_16531736.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117196_21631736.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000297504+117296_31631736.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116145_16531719.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116196_21631719.0TransmembraneHelical
HgeneABCB8chr7:150725697chr7:150706018ENST00000358849+116296_31631719.0TransmembraneHelical
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627520_7037041204.0DomainFlavodoxin-like
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627520_7037041204.0DomainFlavodoxin-like
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627649_6807041204.0Nucleotide bindingFMN
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627649_6807041204.0Nucleotide bindingFMN
TgeneNOS3chr7:150725696chr7:150706017ENST000002974941627491_5107041204.0RegionCalmodulin-binding
TgeneNOS3chr7:150725697chr7:150706018ENST000002974941627491_5107041204.0RegionCalmodulin-binding


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Fusion Gene Sequence for ABCB8-NOS3


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 ABCB8-NOS3


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
TgeneNOS3chr7:150725696chr7:150706017ENST0000048452401498_4860.0630.0NOSIP
TgeneNOS3chr7:150725697chr7:150706018ENST0000048452401498_4860.0630.0NOSIP


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
TgeneNOS3chr7:150725696chr7:150706017ENST00000297494162798_486704.01204.0NOSIP
TgeneNOS3chr7:150725697chr7:150706018ENST00000297494162798_486704.01204.0NOSIP


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 ABCB8-NOS3


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 ABCB8-NOS3


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