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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:ASAH1-TRAPPC9

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ASAH1-TRAPPC9
FusionPDB ID: 6946
FusionGDB2.0 ID: 6946
HgeneTgene
Gene symbol

ASAH1

TRAPPC9

Gene ID

427

83696

Gene nameN-acylsphingosine amidohydrolase 1trafficking protein particle complex 9
SynonymsAC|ACDase|ASAH|PHP|PHP32|SMAPMEIBP|IKBKBBP|MRT13|NIBP|T1|TRS120
Cytomap

8p22

8q24.3

Type of geneprotein-codingprotein-coding
Descriptionacid ceramidaseN-acylethanolamine hydrolase ASAH1N-acylsphingosine amidohydrolase (acid ceramidase) 1acid CDaseacylsphingosine deacylaseputative 32 kDa heart proteintrafficking protein particle complex subunit 9IKK2 binding proteinNIK and IKK-beta binding proteinNIK- and IKBKB-binding proteinTRAPP 120 kDa subunittularik gene 1 protein
Modification date2020031320200313
UniProtAcc

Q13510

Main function of 5'-partner protein: FUNCTION: Lysosomal ceramidase that hydrolyzes sphingolipid ceramides into sphingosine and free fatty acids at acidic pH (PubMed:10610716, PubMed:7744740, PubMed:15655246, PubMed:11451951). Ceramides, sphingosine, and its phosphorylated form sphingosine-1-phosphate are bioactive lipids that mediate cellular signaling pathways regulating several biological processes including cell proliferation, apoptosis and differentiation (PubMed:10610716). Has a higher catalytic efficiency towards C12-ceramides versus other ceramides (PubMed:7744740, PubMed:15655246). Also catalyzes the reverse reaction allowing the synthesis of ceramides from fatty acids and sphingosine (PubMed:12764132, PubMed:12815059). For the reverse synthetic reaction, the natural sphingosine D-erythro isomer is more efficiently utilized as a substrate compared to D-erythro-dihydrosphingosine and D-erythro-phytosphingosine, while the fatty acids with chain lengths of 12 or 14 carbons are the most efficiently used (PubMed:12764132). Has also an N-acylethanolamine hydrolase activity (PubMed:15655246). By regulating the levels of ceramides, sphingosine and sphingosine-1-phosphate in the epidermis, mediates the calcium-induced differentiation of epidermal keratinocytes (PubMed:17713573). Also indirectly regulates tumor necrosis factor/TNF-induced apoptosis (By similarity). By regulating the intracellular balance between ceramides and sphingosine, in adrenocortical cells, probably also acts as a regulator of steroidogenesis (PubMed:22261821). {ECO:0000250|UniProtKB:Q9WV54, ECO:0000269|PubMed:10610716, ECO:0000269|PubMed:11451951, ECO:0000269|PubMed:12764132, ECO:0000269|PubMed:12815059, ECO:0000269|PubMed:15655246, ECO:0000269|PubMed:17713573, ECO:0000269|PubMed:22261821, ECO:0000269|PubMed:7744740, ECO:0000303|PubMed:10610716}.; FUNCTION: [Isoform 2]: May directly regulate steroidogenesis by binding the nuclear receptor NR5A1 and negatively regulating its transcriptional activity. {ECO:0000305|PubMed:22927646}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000262097, ENST00000314146, 
ENST00000381733, ENST00000417108, 
ENST00000520781, ENST00000520051, 
ENST00000522504, ENST00000389327, 
ENST00000389328, ENST00000438773, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 16 X 7=168020 X 19 X 14=5320
# samples 1640
** MAII scorelog2(16/1680*10)=-3.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(40/5320*10)=-3.73335434061383
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ASAH1 [Title/Abstract] AND TRAPPC9 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ASAH1 [Title/Abstract] AND TRAPPC9 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ASAH1(17924729)-TRAPPC9(140744445), # 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
HgeneASAH1

GO:0046512

sphingosine biosynthetic process

12815059

HgeneASAH1

GO:0046513

ceramide biosynthetic process

12764132|12815059

HgeneASAH1

GO:0046514

ceramide catabolic process

12815059



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/chr8:17924729/chr8:140744445)
- 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 ASAH1 (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 TRAPPC9 (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)
ENST00000262097ASAH1chr817924729-ENST00000389327TRAPPC9chr8140744445-1804694151085356
ENST00000262097ASAH1chr817924729-ENST00000389328TRAPPC9chr8140744445-1804694151085356
ENST00000262097ASAH1chr817924729-ENST00000438773TRAPPC9chr8140744445-1802694151085356
ENST00000381733ASAH1chr817924729-ENST00000389327TRAPPC9chr8140744445-17075975988327
ENST00000381733ASAH1chr817924729-ENST00000389328TRAPPC9chr8140744445-17075975988327
ENST00000381733ASAH1chr817924729-ENST00000438773TRAPPC9chr8140744445-17055975988327
ENST00000417108ASAH1chr817924729-ENST00000389327TRAPPC9chr8140744445-152841821809262
ENST00000417108ASAH1chr817924729-ENST00000389328TRAPPC9chr8140744445-152841821809262
ENST00000417108ASAH1chr817924729-ENST00000438773TRAPPC9chr8140744445-152641821809262
ENST00000520781ASAH1chr817924729-ENST00000389327TRAPPC9chr8140744445-1804694151085356
ENST00000520781ASAH1chr817924729-ENST00000389328TRAPPC9chr8140744445-1804694151085356
ENST00000520781ASAH1chr817924729-ENST00000438773TRAPPC9chr8140744445-1802694151085356
ENST00000314146ASAH1chr817924729-ENST00000389327TRAPPC9chr8140744445-165854822939305
ENST00000314146ASAH1chr817924729-ENST00000389328TRAPPC9chr8140744445-165854822939305
ENST00000314146ASAH1chr817924729-ENST00000438773TRAPPC9chr8140744445-165654822939305

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
ENST00000262097ENST00000389327ASAH1chr817924729-TRAPPC9chr8140744445-0.0121545660.9878455
ENST00000262097ENST00000389328ASAH1chr817924729-TRAPPC9chr8140744445-0.0121545660.9878455
ENST00000262097ENST00000438773ASAH1chr817924729-TRAPPC9chr8140744445-0.0121736050.9878264
ENST00000381733ENST00000389327ASAH1chr817924729-TRAPPC9chr8140744445-0.056036330.9439637
ENST00000381733ENST00000389328ASAH1chr817924729-TRAPPC9chr8140744445-0.056036330.9439637
ENST00000381733ENST00000438773ASAH1chr817924729-TRAPPC9chr8140744445-0.0560599860.94394
ENST00000417108ENST00000389327ASAH1chr817924729-TRAPPC9chr8140744445-0.0140753940.98592454
ENST00000417108ENST00000389328ASAH1chr817924729-TRAPPC9chr8140744445-0.0140753940.98592454
ENST00000417108ENST00000438773ASAH1chr817924729-TRAPPC9chr8140744445-0.0141133610.9858867
ENST00000520781ENST00000389327ASAH1chr817924729-TRAPPC9chr8140744445-0.0121545660.9878455
ENST00000520781ENST00000389328ASAH1chr817924729-TRAPPC9chr8140744445-0.0121545660.9878455
ENST00000520781ENST00000438773ASAH1chr817924729-TRAPPC9chr8140744445-0.0121736050.9878264
ENST00000314146ENST00000389327ASAH1chr817924729-TRAPPC9chr8140744445-0.087612590.91238743
ENST00000314146ENST00000389328ASAH1chr817924729-TRAPPC9chr8140744445-0.087612590.91238743
ENST00000314146ENST00000438773ASAH1chr817924729-TRAPPC9chr8140744445-0.088220420.9117795

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 ASAH1-TRAPPC9

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ASAH1chr817924729TRAPPC9chr8140744445418132EMKGIAAVTDIPLDVLVDGQPCDREA
ASAH1chr817924729TRAPPC9chr8140744445548175EMKGIAAVTDIPLDVLVDGQPCDREA
ASAH1chr817924729TRAPPC9chr8140744445597197EMKGIAAVTDIPLDVLVDGQPCDREA
ASAH1chr817924729TRAPPC9chr8140744445694226EMKGIAAVTDIPLDVLVDGQPCDREA

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Potential FusionNeoAntigen Information of ASAH1-TRAPPC9 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.
ASAH1-TRAPPC9_17924729_140744445.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)
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:38AVTDIPLDV0.96730.6707615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:20AVTDIPLDV0.94030.5676615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:21AVTDIPLDV0.93510.7023615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:35AVTDIPLDV0.92190.5763615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-B13:02AVTDIPLDV0.0830.8916615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C05:09VTDIPLDV10.9764715
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:15VTDIPLDV0.99970.9857715
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C05:09VTDIPLDVL0.99990.9646716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:07VTDIPLDVL0.99990.8451716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:10VTDIPLDVL0.99990.8164716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:15VTDIPLDVL0.99980.9796716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C15:06AVTDIPLDV0.99030.9538615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:06VTDIPLDVL0.98530.9381716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:04VTDIPLDVL0.95550.9819716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:13VTDIPLDVL0.95550.9819716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:14VTDIPLDVL0.93150.8117716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:03VTDIPLDVL0.8290.9864716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:07VTDIPLDVL0.75330.6871716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C02:06AVTDIPLDV0.41730.973615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C05:01VTDIPLDV10.9764715
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:03VTDIPLDV10.922715
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:02VTDIPLDV0.99970.9857715
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:01VTDIPLDVL0.99990.8451716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C04:03VTDIPLDVL0.99990.8906716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C05:01VTDIPLDVL0.99990.9646716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C01:03VTDIPLDVL0.99980.9538716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:02VTDIPLDVL0.99980.9796716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C18:01VTDIPLDVL0.99980.8512716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C15:02AVTDIPLDV0.99480.9401615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C15:05AVTDIPLDV0.99340.9597615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C15:05VTDIPLDVL0.99190.9468716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:14AVTDIPLDV0.93560.5706615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A02:06AVTDIPLDV0.93510.7023615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C03:06VTDIPLDVL0.9280.9932716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-A69:01AVTDIPLDV0.89920.746615
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C08:01VTDIPLDVL0.8290.9864716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-C17:01VTDIPLDVL0.56480.9318716
ASAH1-TRAPPC9chr817924729chr8140744445694HLA-B07:13VTDIPLDVL0.03320.8829716

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Potential FusionNeoAntigen Information of ASAH1-TRAPPC9 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.
ASAH1-TRAPPC9_17924729_140744445.msa

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)
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1410EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1410MKGIAAVTDIPLDVL116
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1503EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1507EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1523EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1525EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1548EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1615EMKGIAAVTDIPLDV015
ASAH1-TRAPPC9chr817924729chr8140744445694DRB1-1615MKGIAAVTDIPLDVL116

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Fusion breakpoint peptide structures of ASAH1-TRAPPC9

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
714AVTDIPLDVLVDGQASAH1TRAPPC9chr817924729chr8140744445694

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ASAH1-TRAPPC9

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-B14:023BVN714AVTDIPLDVLVDGQ-6.9888-7.1022
HLA-B14:023BVN714AVTDIPLDVLVDGQ-3.71338-4.74868
HLA-B52:013W39714AVTDIPLDVLVDGQ-5.59342-6.62872
HLA-B52:013W39714AVTDIPLDVLVDGQ-5.47943-5.59283
HLA-A24:025HGA714AVTDIPLDVLVDGQ-6.88714-7.00054
HLA-A24:025HGA714AVTDIPLDVLVDGQ-6.46973-7.50503
HLA-B44:053DX8714AVTDIPLDVLVDGQ-6.00524-6.11864
HLA-B44:053DX8714AVTDIPLDVLVDGQ-5.7663-6.8016

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Vaccine Design for the FusionNeoAntigens of ASAH1-TRAPPC9

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
ASAH1-TRAPPC9chr817924729chr8140744445615AVTDIPLDVCTGTTACTGATATACCTTTAGATGTGC
ASAH1-TRAPPC9chr817924729chr8140744445715VTDIPLDVTTACTGATATACCTTTAGATGTGC
ASAH1-TRAPPC9chr817924729chr8140744445716VTDIPLDVLTTACTGATATACCTTTAGATGTGCTGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ASAH1-TRAPPC9chr817924729chr8140744445015EMKGIAAVTDIPLDVAAATGAAGGGTATTGCCGCTGTTACTGATATACCTTTAGATGTGC
ASAH1-TRAPPC9chr817924729chr8140744445116MKGIAAVTDIPLDVLTGAAGGGTATTGCCGCTGTTACTGATATACCTTTAGATGTGCTGG

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Information of the samples that have these potential fusion neoantigens of ASAH1-TRAPPC9

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
STADASAH1-TRAPPC9chr817924729ENST00000262097chr8140744445ENST00000389327TCGA-CD-8534-01A

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Potential target of CAR-T therapy development for ASAH1-TRAPPC9

check button Predicted 3D structure. We used RoseTTAFold.

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

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

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Related Drugs to ASAH1-TRAPPC9

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 ASAH1-TRAPPC9

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