FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ATP8B1-COG7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP8B1-COG7
FusionPDB ID: 8249
FusionGDB2.0 ID: 8249
HgeneTgene
Gene symbol

ATP8B1

COG7

Gene ID

5205

91949

Gene nameATPase phospholipid transporting 8B1component of oligomeric golgi complex 7
SynonymsATPIC|BRIC|FIC1|ICP1|PFIC|PFIC1CDG2E
Cytomap

18q21.31

16p12.2

Type of geneprotein-codingprotein-coding
Descriptionphospholipid-transporting ATPase ICATPase, aminophospholipid transporter, class I, type 8B, member 1ATPase, class I, type 8B, member 1E1-E2 ATPaseP4-ATPase flippase complex alpha subunit ATP8B1familial intrahepatic cholestasis type 1probable phosphoconserved oligomeric Golgi complex subunit 7COG complex subunit 7
Modification date2020031320200313
UniProtAcc

O43520

Main function of 5'-partner protein: FUNCTION: Catalytic component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of phospholipids, in particular phosphatidylcholines (PC), from the outer to the inner leaflet of the plasma membrane (PubMed:25315773, PubMed:17948906). May participate in the establishment of the canalicular membrane integrity by ensuring asymmetric distribution of phospholipids in the canicular membrane (By similarity). Thus may have a role in the regulation of bile acids transport into the canaliculus, uptake of bile acids from intestinal contents into intestinal mucosa or both and protect hepatocytes from bile salts (By similarity). Involved in the microvillus formation in polarized epithelial cells; the function seems to be independent from its flippase activity (PubMed:20512993). Participates in correct apical membrane localization of CDC42, CFTR and SLC10A2 (PubMed:25239307, PubMed:27301931). Enables CDC42 clustering at the apical membrane during enterocyte polarization through the interaction between CDC42 polybasic region and negatively charged membrane lipids provided by ATP8B1 (By similarity). Together with TMEM30A is involved in uptake of the synthetic drug alkylphospholipid perifosine (PubMed:20510206). Required for the preservation of cochlear hair cells in the inner ear (By similarity). May act as cardiolipin transporter during inflammatory injury (By similarity). {ECO:0000250|UniProtKB:Q148W0, ECO:0000269|PubMed:17948906, ECO:0000269|PubMed:20510206, ECO:0000269|PubMed:20512993, ECO:0000269|PubMed:25239307, ECO:0000269|PubMed:27301931}.

P83436

Main function of 5'-partner protein: FUNCTION: Required for normal Golgi function. {ECO:0000269|PubMed:11980916}.
Ensembl transtripts involved in fusion geneENST idsENST00000283684, ENST00000536015, 
ENST00000589147, 
ENST00000569635, 
ENST00000307149, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 12 X 4=5288 X 6 X 5=240
# samples 127
** MAII scorelog2(12/528*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/240*10)=-1.77760757866355
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ATP8B1 [Title/Abstract] AND COG7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATP8B1 [Title/Abstract] AND COG7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP8B1(55317598)-COG7(23428442), # samples:1
Anticipated loss of major functional domain due to fusion event.ATP8B1-COG7 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ATP8B1-COG7 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneATP8B1

GO:0006855

drug transmembrane transport

20510206

HgeneATP8B1

GO:0045332

phospholipid translocation

20510206



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/chr18:55317598/chr16:23428442)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across ATP8B1 (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 COG7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

Fusion Amino Acid Sequences


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)
ENST00000283684ATP8B1chr1855317598-ENST00000307149COG7chr1623428442-51343531047061568

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
ENST00000283684ENST00000307149ATP8B1chr1855317598-COG7chr1623428442-0.0003817270.9996183

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

Top

Fusion Protein Breakpoint Sequences for ATP8B1-COG7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATP8B1chr1855317598COG7chr162342844235311175IRFLSMTIWPSESDKEHGEVIDCVQE

Top

Potential FusionNeoAntigen Information of ATP8B1-COG7 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
ATP8B1-COG7_55317598_23428442.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
ATP8B1-COG7chr1855317598chr16234284423531HLA-B35:01WPSESDKEH0.96830.9489817
ATP8B1-COG7chr1855317598chr16234284423531HLA-C05:09ESDKEHGEV0.99970.86371120
ATP8B1-COG7chr1855317598chr16234284423531HLA-C08:15ESDKEHGEV0.99930.91551120
ATP8B1-COG7chr1855317598chr16234284423531HLA-C05:01ESDKEHGEV0.99970.86371120
ATP8B1-COG7chr1855317598chr16234284423531HLA-C08:02ESDKEHGEV0.99930.91551120
ATP8B1-COG7chr1855317598chr16234284423531HLA-B35:77WPSESDKEH0.96830.9489817

Top

Potential FusionNeoAntigen Information of ATP8B1-COG7 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

Top

Fusion breakpoint peptide structures of ATP8B1-COG7

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
9419TIWPSESDKEHGEVATP8B1COG7chr1855317598chr16234284423531

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATP8B1-COG7

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN9419TIWPSESDKEHGEV-7.15543-7.26883
HLA-B14:023BVN9419TIWPSESDKEHGEV-4.77435-5.80965
HLA-B52:013W399419TIWPSESDKEHGEV-6.80875-6.92215
HLA-B52:013W399419TIWPSESDKEHGEV-4.20386-5.23916
HLA-A11:014UQ29419TIWPSESDKEHGEV-7.5194-8.5547
HLA-A11:014UQ29419TIWPSESDKEHGEV-6.9601-7.0735
HLA-A24:025HGA9419TIWPSESDKEHGEV-7.52403-7.63743
HLA-A24:025HGA9419TIWPSESDKEHGEV-5.82433-6.85963
HLA-B27:056PYJ9419TIWPSESDKEHGEV-3.28285-4.31815
HLA-B44:053DX89419TIWPSESDKEHGEV-5.91172-6.94702
HLA-B44:053DX89419TIWPSESDKEHGEV-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of ATP8B1-COG7

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
ATP8B1-COG7chr1855317598chr16234284421120ESDKEHGEVGATAAGGAGCATGGGGAAGTGATTGAC
ATP8B1-COG7chr1855317598chr1623428442817WPSESDKEHTCAGAAAGTGATAAGGAGCATGGGGAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

Top

Information of the samples that have these potential fusion neoantigens of ATP8B1-COG7

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
BRCAATP8B1-COG7chr1855317598ENST00000283684chr1623428442ENST00000307149TCGA-AN-A0XT

Top

Potential target of CAR-T therapy development for ATP8B1-COG7

check button Predicted 3D structure. We used RoseTTAFold.
56_ATP8B1-COG7_t000_.e2e.pdb


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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-26271033_105411771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-26271069_109111771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-26271098_111811771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627109_13011771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-26271139_116311771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627137_15611771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627341_36211771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627390_41111771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627950_97011771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000283684-2627983_100211771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-27281033_105411771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-27281069_109111771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-27281098_111811771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728109_13011771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-27281139_116311771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728137_15611771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728341_36211771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728390_41111771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728950_97011771252.0TransmembraneHelical
HgeneATP8B1chr18:55317598chr16:23428442ENST00000536015-2728983_100211771252.0TransmembraneHelical

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result
ATP8B1chr1855317598ENST00000283684COG7chr1623428442ENST00000307149

Top

Related Drugs to ATP8B1-COG7

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

Top

Related Diseases to ATP8B1-COG7

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