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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:ATP11A-EXOC6B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP11A-EXOC6B
FusionPDB ID: 7713
FusionGDB2.0 ID: 7713
HgeneTgene
Gene symbol

ATP11A

EXOC6B

Gene ID

23250

23233

Gene nameATPase phospholipid transporting 11Aexocyst complex component 6B
SynonymsATPIH|ATPISSEC15B|SEC15L2|SEMDJL3
Cytomap

13q34

2p13.2

Type of geneprotein-codingprotein-coding
Descriptionprobable phospholipid-transporting ATPase IHATPase, class VI, type 11AP4-ATPase flippase complex alpha subunit ATP11Aphospholipid-translocating ATPasepotential phospholipid-transporting ATPase IHexocyst complex component 6BSEC15 homolog BSEC15-like protein 2exocyst complex component Sec15B
Modification date2020031320200313
UniProtAcc

Q6ZP68

Q9Y2D4

Ensembl transtripts involved in fusion geneENST idsENST00000283558, ENST00000375630, 
ENST00000375645, ENST00000487903, 
ENST00000419448, 
ENST00000410104, 
ENST00000490919, ENST00000272427, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 11 X 16=352010 X 8 X 6=480
# samples 3111
** MAII scorelog2(31/3520*10)=-3.50523530825042
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/480*10)=-2.12553088208386
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ATP11A [Title/Abstract] AND EXOC6B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP11A(113439571)-EXOC6B(72606999), # 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

check buttonFusion gene breakpoints across ATP11A (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 EXOC6B (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
ChimerDB4Non-CancerTCGA-HU-A4GP-11AATP11Achr13

113439571

+EXOC6Bchr2

72606999

-


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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)
ENST00000283558ATP11Achr13113439571+ENST00000272427EXOC6Bchr272606999-405725055705216
ENST00000375630ATP11Achr13113439571+ENST00000272427EXOC6Bchr272606999-405725055705216
ENST00000487903ATP11Achr13113439571+ENST00000272427EXOC6Bchr272606999-405725055705216
ENST00000375645ATP11Achr13113439571+ENST00000272427EXOC6Bchr272606999-405725055705216

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
ENST00000283558ENST00000272427ATP11Achr13113439571+EXOC6Bchr272606999-0.0049120440.9950879
ENST00000375630ENST00000272427ATP11Achr13113439571+EXOC6Bchr272606999-0.0049120440.9950879
ENST00000487903ENST00000272427ATP11Achr13113439571+EXOC6Bchr272606999-0.0049120440.9950879
ENST00000375645ENST00000272427ATP11Achr13113439571+EXOC6Bchr272606999-0.0049120440.9950879

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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

>7713_7713_1_ATP11A-EXOC6B_ATP11A_chr13_113439571_ENST00000283558_EXOC6B_chr2_72606999_ENST00000272427_length(amino acids)=216AA_BP=65
MNGGAGAAGGAMDCSLVRTLVHRYCAGEENWVDSRTIYVGHREPPPGAEAYIPQRYPDNRIVSSKGKVAQTACMSACKHLATSLMQLLLE
AEVRQLTLGALQQFNLDVRECEQFARSGPVPGFQEDTLQLAFIDLRQLLDLFIQWDWSTYLADYGQPNCKYLRVNPVTALTLLEKMKDTS

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

>7713_7713_2_ATP11A-EXOC6B_ATP11A_chr13_113439571_ENST00000375630_EXOC6B_chr2_72606999_ENST00000272427_length(amino acids)=216AA_BP=65
MNGGAGAAGGAMDCSLVRTLVHRYCAGEENWVDSRTIYVGHREPPPGAEAYIPQRYPDNRIVSSKGKVAQTACMSACKHLATSLMQLLLE
AEVRQLTLGALQQFNLDVRECEQFARSGPVPGFQEDTLQLAFIDLRQLLDLFIQWDWSTYLADYGQPNCKYLRVNPVTALTLLEKMKDTS

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

>7713_7713_3_ATP11A-EXOC6B_ATP11A_chr13_113439571_ENST00000375645_EXOC6B_chr2_72606999_ENST00000272427_length(amino acids)=216AA_BP=65
MNGGAGAAGGAMDCSLVRTLVHRYCAGEENWVDSRTIYVGHREPPPGAEAYIPQRYPDNRIVSSKGKVAQTACMSACKHLATSLMQLLLE
AEVRQLTLGALQQFNLDVRECEQFARSGPVPGFQEDTLQLAFIDLRQLLDLFIQWDWSTYLADYGQPNCKYLRVNPVTALTLLEKMKDTS

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

>7713_7713_4_ATP11A-EXOC6B_ATP11A_chr13_113439571_ENST00000487903_EXOC6B_chr2_72606999_ENST00000272427_length(amino acids)=216AA_BP=65
MNGGAGAAGGAMDCSLVRTLVHRYCAGEENWVDSRTIYVGHREPPPGAEAYIPQRYPDNRIVSSKGKVAQTACMSACKHLATSLMQLLLE
AEVRQLTLGALQQFNLDVRECEQFARSGPVPGFQEDTLQLAFIDLRQLLDLFIQWDWSTYLADYGQPNCKYLRVNPVTALTLLEKMKDTS

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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/chr13:113439571/chr2:72606999)
- 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
ATP11A

Q6ZP68

EXOC6B

Q9Y2D4

FUNCTION: Component of the exocyst complex involved in the docking of exocytic vesicles with fusion sites on the plasma membrane.

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
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291024_102954.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291051_106854.01135.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291094_113454.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229111_29654.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291_6154.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229319_34954.01135.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229373_88154.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+22983_8854.01135.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229903_91454.01135.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229935_96454.01135.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229987_100054.01135.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301024_102954.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301051_106854.02857.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301094_113454.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230111_29654.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301_6154.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230319_34954.02857.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230373_88154.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+23083_8854.02857.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230903_91454.02857.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230935_96454.02857.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230987_100054.02857.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301024_102954.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301051_106854.02878.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301094_113454.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230111_29654.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301_6154.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230319_34954.02878.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230373_88154.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+23083_8854.02878.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230903_91454.02878.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230935_96454.02878.0Topological domainCytoplasmic
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230987_100054.02878.0Topological domainExtracellular
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291001_102354.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291030_105054.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+2291069_109354.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229297_31854.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229350_37254.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+22962_8254.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229882_90254.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+22989_11054.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229915_93454.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000283558+229965_98654.01135.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301001_102354.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301030_105054.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+2301069_109354.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230297_31854.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230350_37254.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+23062_8254.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230882_90254.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+23089_11054.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230915_93454.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000375645+230965_98654.02857.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301001_102354.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301030_105054.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+2301069_109354.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230297_31854.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230350_37254.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+23062_8254.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230882_90254.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+23089_11054.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230915_93454.02878.0TransmembraneHelical
HgeneATP11Achr13:113439571chr2:72606999ENST00000487903+230965_98654.02878.0TransmembraneHelical
TgeneEXOC6Bchr13:113439571chr2:72606999ENST00000272427172250_119660.0812.0Coiled coilOntology_term=ECO:0000255


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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
ATP11A
EXOC6B


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 ATP11A-EXOC6B


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 ATP11A-EXOC6B


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