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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:ABCC3-TMEM104

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ABCC3-TMEM104
FusionPDB ID: 263
FusionGDB2.0 ID: 263
HgeneTgene
Gene symbol

ABCC3

TMEM104

Gene ID

8714

54868

Gene nameATP binding cassette subfamily C member 3transmembrane protein 104
SynonymsABC31|EST90757|MLP2|MOAT-D|MRP3|cMOAT2-
Cytomap

17q21.33

17q25.1

Type of geneprotein-codingprotein-coding
Descriptioncanalicular multispecific organic anion transporter 2ATP-binding cassette sub-family C member 3ATP-binding cassette, sub-family C (CFTR/MRP), member 3canicular multispecific organic anion transportermulti-specific organic anion transporter Dmultidrugtransmembrane protein 104
Modification date2020031320200313
UniProtAcc

O15438

Main function of 5'-partner protein: FUNCTION: ATP-dependent transporter of the ATP-binding cassette (ABC) family that bind and hydrolyze ATP to enable active transport of various substrates including many drugs, toxicants and endogenous compound across cell membranes (PubMed:11581266, PubMed:15083066, PubMed:10359813). Transports glucuronide conjugates such as bilirubin diglucuronide, estradiol-17-beta-o-glucuronide and GSH conjugates such as leukotriene C4 (LTC4) (PubMed:15083066, PubMed:11581266). Transports also various bile salts (taurocholate, glycocholate, taurochenodeoxycholate-3-sulfate, taurolithocholate- 3-sulfate) (By similarity). Does not contribute substantially to bile salt physiology but provides an alternative route for the export of bile acids and glucuronides from cholestatic hepatocytes (By similarity). Can confers resistance to various anticancer drugs, methotrexate, tenoposide and etoposide, by decreasing accumulation of these drugs in cells (PubMed:11581266, PubMed:10359813). {ECO:0000250|UniProtKB:O88563, ECO:0000269|PubMed:10359813, ECO:0000269|PubMed:11581266, ECO:0000269|PubMed:15083066}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000285238, ENST00000427699, 
ENST00000515707, ENST00000510891, 
ENST00000584171, ENST00000335464, 
ENST00000417024, ENST00000582330, 
ENST00000582773, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 12 X 7=13448 X 7 X 7=392
# samples 189
** MAII scorelog2(18/1344*10)=-2.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/392*10)=-2.12285674778553
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ABCC3 [Title/Abstract] AND TMEM104 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ABCC3 [Title/Abstract] AND TMEM104 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ABCC3(48712342)-TMEM104(72815889), # samples:1
Anticipated loss of major functional domain due to fusion event.ABCC3-TMEM104 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.
ABCC3-TMEM104 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
HgeneABCC3

GO:0042908

xenobiotic transport

18698235|19334674



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/chr17:48712342/chr17:72815889)
- 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 ABCC3 (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 TMEM104 (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)
ENST00000285238ABCC3chr1748712342+ENST00000335464TMEM104chr1772815889+407212559979306
ENST00000285238ABCC3chr1748712342+ENST00000417024TMEM104chr1772815889+1085125340879179
ENST00000285238ABCC3chr1748712342+ENST00000582773TMEM104chr1772815889+1084125340879179
ENST00000285238ABCC3chr1748712342+ENST00000582330TMEM104chr1772815889+404612511922397
ENST00000515707ABCC3chr1748712342+ENST00000335464TMEM104chr1772815889+40419449948299
ENST00000515707ABCC3chr1748712342+ENST00000417024TMEM104chr1772815889+105494309848179
ENST00000515707ABCC3chr1748712342+ENST00000582773TMEM104chr1772815889+105394309848179
ENST00000515707ABCC3chr1748712342+ENST00000582330TMEM104chr1772815889+40159411611387
ENST00000427699ABCC3chr1748712342+ENST00000335464TMEM104chr1772815889+407212559979306
ENST00000427699ABCC3chr1748712342+ENST00000417024TMEM104chr1772815889+1085125340879179
ENST00000427699ABCC3chr1748712342+ENST00000582773TMEM104chr1772815889+1084125340879179
ENST00000427699ABCC3chr1748712342+ENST00000582330TMEM104chr1772815889+404612511922397

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
ENST00000285238ENST00000335464ABCC3chr1748712342+TMEM104chr1772815889+0.032514830.96748513
ENST00000285238ENST00000417024ABCC3chr1748712342+TMEM104chr1772815889+0.323717030.676283
ENST00000285238ENST00000582773ABCC3chr1748712342+TMEM104chr1772815889+0.32471240.6752876
ENST00000285238ENST00000582330ABCC3chr1748712342+TMEM104chr1772815889+0.035654460.9643456
ENST00000515707ENST00000335464ABCC3chr1748712342+TMEM104chr1772815889+0.032323620.96767634
ENST00000515707ENST00000417024ABCC3chr1748712342+TMEM104chr1772815889+0.393677950.6063221
ENST00000515707ENST00000582773ABCC3chr1748712342+TMEM104chr1772815889+0.394919720.6050803
ENST00000515707ENST00000582330ABCC3chr1748712342+TMEM104chr1772815889+0.0354788230.9645211
ENST00000427699ENST00000335464ABCC3chr1748712342+TMEM104chr1772815889+0.032514830.96748513
ENST00000427699ENST00000417024ABCC3chr1748712342+TMEM104chr1772815889+0.323717030.676283
ENST00000427699ENST00000582773ABCC3chr1748712342+TMEM104chr1772815889+0.32471240.6752876
ENST00000427699ENST00000582330ABCC3chr1748712342+TMEM104chr1772815889+0.035654460.9643456

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 ABCC3-TMEM104

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ABCC3chr1748712342TMEM104chr177281588912522ALCGSGELGSKFWAIFTLLLGPFTFF
ABCC3chr1748712342TMEM104chr17728158899415ALCGSGELGSKFWAIFTLLLGPFTFF

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Potential FusionNeoAntigen Information of ABCC3-TMEM104 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.
ABCC3-TMEM104_48712342_72815889.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)
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:24SKFWAIFTL0.99440.6096918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B27:04SKFWAIFTL0.99170.7623918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:06SKFWAIFTL0.99020.7789918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B45:01GELGSKFWA0.98590.9929514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:01SKFWAIFTL0.98590.9146918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B50:02GELGSKFWA0.98420.8988514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B38:01SKFWAIFTL0.97440.9793918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B38:02SKFWAIFTL0.97280.979918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B14:02SKFWAIFTL0.97220.8789918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B14:01SKFWAIFTL0.97220.8789918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:13SKFWAIFTL0.96810.9297918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B08:01ELGSKFWAI0.94710.9576615
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B08:09ELGSKFWAI0.90870.9303615
ABCC3-TMEM104chr1748712342chr1772815889125HLA-A02:19ELGSKFWAI0.55270.7962615
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B15:10SKFWAIFTL0.48030.6372918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B15:37SKFWAIFTL0.24990.7663918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B41:01GELGSKFWA0.21410.9962514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B50:01GELGSKFWA0.12870.921514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B52:01SKFWAIFTL0.0470.9896918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B40:06GELGSKFWA0.99410.7991514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:95SKFWAIFTL0.99340.7713918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:09SKFWAIFTL0.98980.7328918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:27SKFWAIFTL0.98780.9627918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:12SKFWAIFTL0.98750.9249918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:05SKFWAIFTL0.98510.9599918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:13SKFWAIFTL0.97610.9182918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:05SKFWAIFTL0.96510.8977918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:10SKFWAIFTL0.92970.9636918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:19SKFWAIFTL0.92960.8283918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:80SKFWAIFTL0.92490.9549918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:67SKFWAIFTL0.92490.9549918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:46SKFWAIFTL0.91010.9075918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B73:01SKFWAIFTL0.72930.7132918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B40:03GELGSKFWAIF0.99970.8977516
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B27:06SKFWAIFTL0.99520.7486918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:01SKFWAIFTL0.99150.7737918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B27:08SKFWAIFTL0.98840.7642918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:02SKFWAIFTL0.98830.9335918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B39:31SKFWAIFTL0.98750.9179918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B27:09SKFWAIFTL0.98290.891918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B38:05SKFWAIFTL0.97440.9793918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B08:18ELGSKFWAI0.94710.9576615
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:02SKFWAIFTL0.92490.9549918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C07:22SKFWAIFTL0.77170.7706918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C06:08SKFWAIFTL0.70040.9915918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B08:12ELGSKFWAI0.61290.9785615
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B15:09SKFWAIFTL0.47050.7957918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C06:17SKFWAIFTL0.20870.9942918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C06:02SKFWAIFTL0.20870.9942918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-C04:04FWAIFTLLL0.1920.92961120
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B15:68SKFWAIFTL0.13570.685918
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B50:04GELGSKFWA0.12870.921514
ABCC3-TMEM104chr1748712342chr1772815889125HLA-B50:05GELGSKFWA0.12870.921514

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Potential FusionNeoAntigen Information of ABCC3-TMEM104 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 ABCC3-TMEM104

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
1895ELGSKFWAIFTLLLABCC3TMEM104chr1748712342chr1772815889125

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ABCC3-TMEM104

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-B14:023BVN1895ELGSKFWAIFTLLL-7.63753-7.75093
HLA-B14:023BVN1895ELGSKFWAIFTLLL-4.36349-5.39879
HLA-B52:013W391895ELGSKFWAIFTLLL-6.74822-6.86162
HLA-B52:013W391895ELGSKFWAIFTLLL-4.96916-6.00446
HLA-A24:025HGA1895ELGSKFWAIFTLLL-8.26666-9.30196
HLA-A24:025HGA1895ELGSKFWAIFTLLL-7.6208-7.7342
HLA-B27:036PZ51895ELGSKFWAIFTLLL0.0420189-0.993281
HLA-B44:053DX81895ELGSKFWAIFTLLL-5.06122-5.17462
HLA-B44:053DX81895ELGSKFWAIFTLLL-4.87073-5.90603

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Vaccine Design for the FusionNeoAntigens of ABCC3-TMEM104

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
ABCC3-TMEM104chr1748712342chr17728158891120FWAIFTLLLTTCTGGGCGATCTTCACTCTCCTCCTC
ABCC3-TMEM104chr1748712342chr1772815889514GELGSKFWAGGGGAGCTCGGCTCCAAGTTCTGGGCG
ABCC3-TMEM104chr1748712342chr1772815889516GELGSKFWAIFGGGGAGCTCGGCTCCAAGTTCTGGGCGATCTTC
ABCC3-TMEM104chr1748712342chr1772815889615ELGSKFWAIGAGCTCGGCTCCAAGTTCTGGGCGATC
ABCC3-TMEM104chr1748712342chr1772815889918SKFWAIFTLTCCAAGTTCTGGGCGATCTTCACTCTC

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 ABCC3-TMEM104

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
STADABCC3-TMEM104chr1748712342ENST00000285238chr1772815889ENST00000335464TCGA-BR-8373-01A

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Potential target of CAR-T therapy development for ABCC3-TMEM104

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
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710234_2540497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710277_2970497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710307_3270497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710355_3750497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710398_4180497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710422_4420497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000335464710471_4910497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710234_2540497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710277_2970497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710307_3270497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710355_3750497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710398_4180497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710422_4420497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582330710471_4910497.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710234_2540315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710277_2970315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710307_3270315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710355_3750315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710398_4180315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710422_4420315.0TransmembraneHelical
TgeneTMEM104chr17:48712342chr17:72815889ENST00000582773710471_4910315.0TransmembraneHelical

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

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Related Drugs to ABCC3-TMEM104

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 ABCC3-TMEM104

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