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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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

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

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

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

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:PGAP1-AOX1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PGAP1-AOX1
FusionPDB ID: 64534
FusionGDB2.0 ID: 64534
HgeneTgene
Gene symbol

PGAP1

AOX1

Gene ID

80055

316

Gene namepost-GPI attachment to proteins inositol deacylase 1aldehyde oxidase 1
SynonymsBst1|ISPD3024|MRT42|SPG67AO|AOH1
Cytomap

2q33.1

2q33.1

Type of geneprotein-codingprotein-coding
DescriptionGPI inositol-deacylasepost-GPI attachment to proteins 1post-GPI attachment to proteins factor 1aldehyde oxidaseazaheterocycle hydroxylase
Modification date2020031320200313
UniProtAcc.

Q06278

Main function of 5'-partner protein: FUNCTION: Oxidase with broad substrate specificity, oxidizing aromatic azaheterocycles, such as N1-methylnicotinamide, N-methylphthalazinium and phthalazine, as well as aldehydes, such as benzaldehyde, retinal, pyridoxal, and vanillin. Plays a key role in the metabolism of xenobiotics and drugs containing aromatic azaheterocyclic substituents. Participates in the bioactivation of prodrugs such as famciclovir, catalyzing the oxidation step from 6-deoxypenciclovir to penciclovir, which is a potent antiviral agent. Is probably involved in the regulation of reactive oxygen species homeostasis. May be a prominent source of superoxide generation via the one-electron reduction of molecular oxygen. Also may catalyze nitric oxide (NO) production via the reduction of nitrite to NO with NADH or aldehyde as electron donor. May play a role in adipogenesis. {ECO:0000269|PubMed:20444863, ECO:0000269|PubMed:22031625, ECO:0000269|PubMed:22279051, ECO:0000269|PubMed:22522748, ECO:0000269|PubMed:22996261, ECO:0000269|PubMed:23857892, ECO:0000269|PubMed:26322824, ECO:0000269|PubMed:7786031, ECO:0000269|PubMed:9224775}.
Ensembl transtripts involved in fusion geneENST idsENST00000354764, ENST00000409475, 
ENST00000409188, ENST00000485830, 
ENST00000485106, ENST00000374700, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 12 X 7=7562 X 2 X 2=8
# samples 102
** MAII scorelog2(10/756*10)=-2.91838623444635
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Fusion gene context

PubMed: PGAP1 [Title/Abstract] AND AOX1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PGAP1 [Title/Abstract] AND AOX1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PGAP1(197740469)-AOX1(201473706), # samples:1
Anticipated loss of major functional domain due to fusion event.PGAP1-AOX1 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.
PGAP1-AOX1 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.
PGAP1-AOX1 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.
PGAP1-AOX1 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
TgeneAOX1

GO:0017144

drug metabolic process

20444863|22031625|22522748|23857892

TgeneAOX1

GO:0055114

oxidation-reduction process

22279051|22996261



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/chr2:197740469/chr2:201473706)
- 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 PGAP1 (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 AOX1 (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 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)
ENST00000354764PGAP1chr2197740469-ENST00000374700AOX1chr2201473706+546315414946501533
ENST00000409475PGAP1chr2197740469-ENST00000374700AOX1chr2201473706+546215404846491533

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
ENST00000354764ENST00000374700PGAP1chr2197740469-AOX1chr2201473706+0.0002340190.99976593
ENST00000409475ENST00000374700PGAP1chr2197740469-AOX1chr2201473706+0.0002338280.9997662

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

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Fusion Protein Breakpoint Sequences for PGAP1-AOX1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PGAP1chr2197740469AOX1chr22014737061540497RYIQLPVTHLFSFGLTLGAGLSLAQV
PGAP1chr2197740469AOX1chr22014737061541497RYIQLPVTHLFSFGLTLGAGLSLAQV

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Potential FusionNeoAntigen Information of PGAP1-AOX1 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.
PGAP1-AOX1_197740469_201473706.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)
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:01THLFSFGL0.99960.8721715
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:22HLFSFGLTL0.98710.664817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:13HLFSFGLTL0.98080.8298817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:67HLFSFGLTL0.97990.6065817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:24HLFSFGLTL0.97990.6065817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:30HLFSFGLTL0.97990.6065817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:60HLFSFGLTL0.97950.5751817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:11HLFSFGLTL0.97840.673817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:27HLFSFGLTL0.97660.7811817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:21HLFSFGLTL0.97570.7402817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:16HLFSFGLTL0.96820.5545817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:38HLFSFGLTL0.96640.7597817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:04HLFSFGLTL0.96110.8513817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:35HLFSFGLTL0.95850.6583817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:17HLFSFGLTL0.95770.6586817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:29HLFSFGLTL0.94060.6171817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:20HLFSFGLTL0.91630.6175817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:19HLFSFGLTL0.86050.5208817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:25HLFSFGLTL0.83360.9388817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:02HLFSFGLTL0.82110.9524817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B14:02HLFSFGLTL0.81460.9632817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B14:01HLFSFGLTL0.81460.9632817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:24HLFSFGLTL0.73290.6962817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A32:13HLFSFGLTL0.68440.879817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:03HLFSFGLTL0.62710.8204817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:10HLFSFGLTL0.47590.6501817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:01HLFSFGLTL0.44610.9771817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:37HLFSFGLTL0.35130.6602817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:13HLFSFGLTL0.31950.9784817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B13:01HLFSFGLTL0.2220.9236817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B13:02HLFSFGLTL0.21640.8387817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B52:01HLFSFGLTL0.05330.9915817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:24THLFSFGLTL0.99920.7076717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:01THLFSFGLTL0.9990.9552717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:06THLFSFGLTL0.99880.8323717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B38:01THLFSFGLTL0.99840.9594717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B38:02THLFSFGLTL0.9980.9671717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:10THLFSFGLTL0.99540.551717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:18THLFSFGLTL0.9790.7082717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:37THLFSFGLTL0.97880.5303717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:05THLFSFGL0.99920.8472715
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:02HLFSFGLTL0.98770.6328817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:05HLFSFGLTL0.98530.7499817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:07HLFSFGLTL0.98110.6289817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:01HLFSFGLTL0.97990.6065817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:07HLFSFGLTL0.94460.9892817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:19HLFSFGLTL0.9070.9886817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C04:06HLFSFGLTL0.89350.9182817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:21HLFSFGLTL0.83260.9378817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:04HLFSFGLTL0.75840.9088817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C07:13HLFSFGLTL0.64440.8748817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C07:29HLFSFGLTL0.57280.9599817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:14HLFSFGLTL0.56060.9894817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:09HLFSFGLTL0.54820.8325817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:05HLFSFGLTL0.35690.936817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B51:07HLFSFGLTL0.05050.9793817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:09THLFSFGLTL0.99930.7827717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:12THLFSFGLTL0.9990.9562717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:05THLFSFGLTL0.99750.9431717
PGAP1-AOX1chr2197740469chr22014737061541HLA-C14:02LFSFGLTL0.92530.9767917
PGAP1-AOX1chr2197740469chr22014737061541HLA-C14:03LFSFGLTL0.92530.9767917
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:03HLFSFGLTL0.98290.7788817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:14HLFSFGLTL0.97630.711817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A02:06HLFSFGLTL0.97570.7402817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:04HLFSFGLTL0.92920.9896817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:03HLFSFGLTL0.92920.9896817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:67HLFSFGLTL0.90730.9845817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:05HLFSFGLTL0.88310.883817
PGAP1-AOX1chr2197740469chr22014737061541HLA-A32:01HLFSFGLTL0.86730.9741817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C04:04HLFSFGLTL0.86430.892817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C03:06HLFSFGLTL0.86050.9902817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:39HLFSFGLTL0.80420.862817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:73HLFSFGLTL0.75940.9719817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:30HLFSFGLTL0.69450.9814817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B35:13HLFSFGLTL0.56840.9671817
PGAP1-AOX1chr2197740469chr22014737061541HLA-C17:01HLFSFGLTL0.52690.7835817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:02HLFSFGLTL0.51980.9806817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:20HLFSFGLTL0.41060.965817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:09HLFSFGLTL0.24870.8779817
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:31THLFSFGLTL0.9990.9556717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B38:05THLFSFGLTL0.99840.9594717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B15:09THLFSFGLTL0.99570.8627717
PGAP1-AOX1chr2197740469chr22014737061541HLA-B39:11THLFSFGLTL0.95020.9328717

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Potential FusionNeoAntigen Information of PGAP1-AOX1 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)

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Fusion breakpoint peptide structures of PGAP1-AOX1

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
10305VTHLFSFGLTLGAGPGAP1AOX1chr2197740469chr22014737061541

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PGAP1-AOX1

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-B14:023BVN10305VTHLFSFGLTLGAG-7.9962-8.1096
HLA-B14:023BVN10305VTHLFSFGLTLGAG-5.70842-6.74372
HLA-B52:013W3910305VTHLFSFGLTLGAG-6.83737-6.95077
HLA-B52:013W3910305VTHLFSFGLTLGAG-4.4836-5.5189
HLA-A11:014UQ210305VTHLFSFGLTLGAG-10.0067-10.1201
HLA-A11:014UQ210305VTHLFSFGLTLGAG-9.03915-10.0745
HLA-A24:025HGA10305VTHLFSFGLTLGAG-6.56204-6.67544
HLA-A24:025HGA10305VTHLFSFGLTLGAG-5.42271-6.45801
HLA-B44:053DX810305VTHLFSFGLTLGAG-7.85648-8.89178
HLA-B44:053DX810305VTHLFSFGLTLGAG-5.3978-5.5112
HLA-B35:011A1N10305VTHLFSFGLTLGAG-6.27422-6.38762
HLA-B35:011A1N10305VTHLFSFGLTLGAG-5.27424-6.30954
HLA-A02:016TDR10305VTHLFSFGLTLGAG-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PGAP1-AOX1

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
PGAP1-AOX1chr2197740469chr2201473706715THLFSFGLCTCATCTTTTTTCCTTTGGACTCA
PGAP1-AOX1chr2197740469chr2201473706717THLFSFGLTLCTCATCTTTTTTCCTTTGGACTCACCCTTG
PGAP1-AOX1chr2197740469chr2201473706817HLFSFGLTLATCTTTTTTCCTTTGGACTCACCCTTG
PGAP1-AOX1chr2197740469chr2201473706917LFSFGLTLTTTTTTCCTTTGGACTCACCCTTG

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

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Information of the samples that have these potential fusion neoantigens of PGAP1-AOX1

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
ESCAPGAP1-AOX1chr2197740469ENST00000354764chr2201473706ENST00000374700TCGA-Q9-A6FW

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Potential target of CAR-T therapy development for PGAP1-AOX1

check button Predicted 3D structure. We used RoseTTAFold.
322_PGAP1-AOX1_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
HgenePGAP1chr2:197740469chr2:201473706ENST00000354764-142712_32475923.0TransmembraneHelical
HgenePGAP1chr2:197740469chr2:201473706ENST00000409475-142012_32475593.0TransmembraneHelical

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
PGAP1chr2197740469ENST00000354764AOX1chr2201473706ENST00000374700

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Related Drugs to PGAP1-AOX1

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 PGAP1-AOX1

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