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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RAC3-ABCA8

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RAC3-ABCA8
FusionPDB ID: 71638
FusionGDB2.0 ID: 71638
HgeneTgene
Gene symbol

RAC3

ABCA8

Gene ID

8202

10351

Gene namenuclear receptor coactivator 3ATP binding cassette subfamily A member 8
SynonymsACTR|AIB-1|AIB1|CAGH16|CTG26|KAT13B|RAC3|SRC-3|SRC3|TNRC14|TNRC16|TRAM-1|bHLHe42|pCIP-
Cytomap

20q13.12

17q24.2

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor coactivator 3CBP-interacting proteinamplified in breast cancer 1 proteinclass E basic helix-loop-helix protein 42receptor-associated coactivator 3steroid receptor coactivator protein 3thyroid hormone receptor activator molecule 1ATP-binding cassette sub-family A member 8ATP-binding cassette, sub-family A (ABC1), member 8
Modification date2020031320200313
UniProtAcc.

O94911

Ensembl transtripts involved in fusion geneENST idsENST00000306897, ENST00000269080, 
ENST00000430352, ENST00000586539, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score1 X 1 X 1=13 X 2 X 2=12
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RAC3 [Title/Abstract] AND ABCA8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RAC3(79989672)-ABCA8(66865920), # samples:3
Anticipated loss of major functional domain due to fusion event.RAC3-ABCA8 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RAC3-ABCA8 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneRAC3

GO:0045944

positive regulation of transcription by RNA polymerase II

9267036

HgeneRAC3

GO:0071392

cellular response to estradiol stimulus

15831516


check buttonFusion gene breakpoints across RAC3 (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 ABCA8 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-AQ-A04H-01BRAC3chr17

79989672

-ABCA8chr17

66865920

-
ChimerDB4BRCATCGA-AQ-A04H-01BRAC3chr17

79989672

+ABCA8chr17

66865920

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000306897RAC3chr1779989672+ENST00000269080ABCA8chr1766865920-120117313840789
ENST00000306897RAC3chr1779989672+ENST00000430352ABCA8chr1766865920-44117313840789
ENST00000306897RAC3chr1779989672+ENST00000586539ABCA8chr1766865920-44117313840789

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
ENST00000306897ENST00000269080RAC3chr1779989672+ABCA8chr1766865920-0.0282440130.97175604
ENST00000306897ENST00000430352RAC3chr1779989672+ABCA8chr1766865920-0.0255893970.9744106
ENST00000306897ENST00000586539RAC3chr1779989672+ABCA8chr1766865920-0.0255893970.9744106

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>71638_71638_1_RAC3-ABCA8_RAC3_chr17_79989672_ENST00000306897_ABCA8_chr17_66865920_ENST00000269080_length(amino acids)=89AA_BP=12

--------------------------------------------------------------

>71638_71638_2_RAC3-ABCA8_RAC3_chr17_79989672_ENST00000306897_ABCA8_chr17_66865920_ENST00000430352_length(amino acids)=89AA_BP=12

--------------------------------------------------------------

>71638_71638_3_RAC3-ABCA8_RAC3_chr17_79989672_ENST00000306897_ABCA8_chr17_66865920_ENST00000586539_length(amino acids)=89AA_BP=12

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr17:79989672/chr17:66865920)
- 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
.ABCA8

O94911

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: [Isoform 1]: Catalyzes the import of organic anions such as taurocholate and estrone sulfate in an ATP-dependent manner (PubMed:12379217). In vitro, also imports ochratoxin A (PubMed:12379217). In addition mediates the cholesterol efflux in an apolipoprotein independent manner an plays a role in sphingomyelin production in oligodendrocytes (PubMed:23560799). {ECO:0000269|PubMed:12379217, ECO:0000269|PubMed:23560799}.; FUNCTION: [Isoform 3]: Catalyzes the cholesterol and taurocholate efflux in an ATP-dependent manner (PubMed:29300488). Through the interaction with ABCA1 potentiates the cholesterol efflux to lipid-free APOA1, in turn regulates high-density lipoprotein cholesterol levels (PubMed:28882873). {ECO:0000269|PubMed:28882873, ECO:0000269|PubMed:29300488}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRAC3chr17:79989672chr17:66865920ENST00000306897+1632_4011.666666666666666193.0MotifEffector region
HgeneRAC3chr17:79989672chr17:66865920ENST00000306897+1610_1711.666666666666666193.0Nucleotide bindingGTP
HgeneRAC3chr17:79989672chr17:66865920ENST00000306897+16115_11811.666666666666666193.0Nucleotide bindingGTP
HgeneRAC3chr17:79989672chr17:66865920ENST00000306897+1657_6111.666666666666666193.0Nucleotide bindingGTP
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381285_15181503.66666666666671582.0DomainABC transporter 2
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438480_7151503.66666666666671582.0DomainABC transporter 1
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381285_15181543.66666666666671622.0DomainABC transporter 2
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438480_7151543.66666666666671622.0DomainABC transporter 1
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381323_13301503.66666666666671582.0Nucleotide bindingATP 2
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438516_5231503.66666666666671582.0Nucleotide bindingATP 1
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381323_13301543.66666666666671622.0Nucleotide bindingATP 2
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438516_5231543.66666666666671622.0Nucleotide bindingATP 1
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381019_10391503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381070_10901503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381106_11261503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381136_11561503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381161_11811503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000026908034381197_12171503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438220_2401503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438268_2881503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438299_3191503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST00000269080343830_501503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438327_3471503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438359_3791503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438397_4171503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000002690803438864_8841503.66666666666671582.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381019_10391543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381070_10901543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381106_11261543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381136_11561543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381161_11811543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST0000043035234381197_12171543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438220_2401543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438268_2881543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438299_3191543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST00000430352343830_501543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438327_3471543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438359_3791543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438397_4171543.66666666666671622.0TransmembraneHelical
TgeneABCA8chr17:79989672chr17:66865920ENST000004303523438864_8841543.66666666666671622.0TransmembraneHelical


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RAC3
ABCA8


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to RAC3-ABCA8


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RAC3-ABCA8


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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