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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:ABCC4-ATP9A (FusionGDB2 ID:HG10257TG10079)

Fusion Gene Summary for ABCC4-ATP9A

check button Fusion gene summary
Fusion gene informationFusion gene name: ABCC4-ATP9A
Fusion gene ID: hg10257tg10079
HgeneTgene
Gene symbol

ABCC4

ATP9A

Gene ID

10257

10079

Gene nameATP binding cassette subfamily C member 4ATPase phospholipid transporting 9A (putative)
SynonymsMOAT-B|MOATB|MRP4ATPIIA
Cytomap('ABCC4')('ATP9A')

13q32.1

20q13.2

Type of geneprotein-codingprotein-coding
Descriptionmultidrug resistance-associated protein 4MRP/cMOAT-related ABC transporterbA464I2.1 (ATP-binding cassette, sub-family C (CFTR/MRP), member 4)canalicular multispecific organic anion transporter (ABC superfamily)multi-specific organic anion transporter probable phospholipid-transporting ATPase IIAATPase type IV, phospholipid-transporting (P-type),(putative)ATPase, class II, type 9Aphospholipid-transporting ATPase IIA
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000376887, ENST00000412704, 
ENST00000431522, ENST00000474158, 
ENST00000536256, ENST00000538287, 
Fusion gene scores* DoF score23 X 21 X 11=531318 X 17 X 7=2142
# samples 2518
** MAII scorelog2(25/5313*10)=-4.40952671281098
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/2142*10)=-3.57288966842058
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ABCC4 [Title/Abstract] AND ATP9A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointABCC4(95673079)-ATP9A(50368628), # 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
HgeneABCC4

GO:0032310

prostaglandin secretion

25173977



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/AAW609388ABCC4chr13

95673079

+ATP9Achr20

50368628

+


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Fusion Gene ORF analysis for ABCC4-ATP9A

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-intronENST00000376887ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000376887ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000376887ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000376887ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000412704ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000412704ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000412704ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000412704ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000431522ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000431522ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000431522ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000431522ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000474158ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000474158ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000474158ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000474158ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000536256ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000536256ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000536256ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000536256ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000538287ENST00000311637ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000538287ENST00000338821ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000538287ENST00000402822ABCC4chr13

95673079

+ATP9Achr20

50368628

+
intron-intronENST00000538287ENST00000477492ABCC4chr13

95673079

+ATP9Achr20

50368628

+

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 ABCC4-ATP9A


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)


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Fusion Protein Features for ABCC4-ATP9A


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/:95673079/:50368628)
- 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
..
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}.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

- 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 ABCC4-ATP9A


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 ABCC4-ATP9A


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 ABCC4-ATP9A


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 ABCC4-ATP9A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneABCC4C0003873Rheumatoid Arthritis1CTD_human
HgeneABCC4C0009241Cognition Disorders1CTD_human
HgeneABCC4C0009402Colorectal Carcinoma1CTD_human
HgeneABCC4C0009404Colorectal Neoplasms1CTD_human
HgeneABCC4C0013146Drug abuse1CTD_human
HgeneABCC4C0013170Drug habituation1CTD_human
HgeneABCC4C0013221Drug toxicity1CTD_human
HgeneABCC4C0013222Drug Use Disorders1CTD_human
HgeneABCC4C0014175Endometriosis1CTD_human
HgeneABCC4C0027627Neoplasm Metastasis1CTD_human
HgeneABCC4C0029231Organic Mental Disorders, Substance-Induced1CTD_human
HgeneABCC4C0033578Prostatic Neoplasms1CTD_human
HgeneABCC4C0038580Substance Dependence1CTD_human
HgeneABCC4C0038586Substance Use Disorders1CTD_human
HgeneABCC4C0041755Adverse reaction to drug1CTD_human
HgeneABCC4C0236969Substance-Related Disorders1CTD_human
HgeneABCC4C0269102Endometrioma1CTD_human
HgeneABCC4C0342257Complications of Diabetes Mellitus1CTD_human
HgeneABCC4C0376358Malignant neoplasm of prostate1CTD_human
HgeneABCC4C0740858Substance abuse problem1CTD_human
HgeneABCC4C1510472Drug Dependence1CTD_human
HgeneABCC4C4316881Prescription Drug Abuse1CTD_human