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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:TAF3-APP

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TAF3-APP
FusionPDB ID: 88780
FusionGDB2.0 ID: 88780
HgeneTgene
Gene symbol

TAF3

APP

Gene ID

83860

351

Gene nameTATA-box binding protein associated factor 3amyloid beta precursor protein
SynonymsTAF140|TAFII-140|TAFII140AAA|ABETA|ABPP|AD1|APPI|CTFgamma|CVAP|PN-II|PN2|preA4
Cytomap

10p14

21q21.3

Type of geneprotein-codingprotein-coding
Descriptiontranscription initiation factor TFIID subunit 3140 kDa TATA box-binding protein-associated factorRNA polymerase II transcription factor TAFII140TAF(II)140TAF3 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 140kDaTBP-associated famyloid-beta precursor proteinalzheimer disease amyloid proteinamyloid beta (A4) precursor proteinamyloid beta A4 proteinamyloid precursor proteinbeta-amyloid peptidebeta-amyloid peptide(1-40)beta-amyloid peptide(1-42)beta-amyloid precursor protei
Modification date2020031320200329
UniProtAcc.

Q8NEU8

Main function of 5'-partner protein: FUNCTION: Multifunctional adapter protein that binds to various membrane receptors, nuclear factors and signaling proteins to regulate many processes, such as cell proliferation, immune response, endosomal trafficking and cell metabolism (PubMed:26583432, PubMed:15016378, PubMed:24879834). Regulates signaling pathway leading to cell proliferation through interaction with RAB5A and subunits of the NuRD/MeCP1 complex (PubMed:15016378). Plays a role in immune response by modulating phagocytosis, inflammatory and innate immune responses. In macrophages, enhances Fc-gamma receptor-mediated phagocytosis through interaction with RAB31 leading to activation of PI3K/Akt signaling. In response to LPS, modulates inflammatory responses by playing a key role on the regulation of TLR4 signaling and in the nuclear translocation of RELA/NF-kappa-B p65 and the secretion of pro- and anti-inflammatory cytokines. Also functions as a negative regulator of innate immune response via inhibition of AKT1 signaling pathway by forming a complex with APPL1 and PIK3R1 (By similarity). Plays a role in endosomal trafficking of TGFBR1 from the endosomes to the nucleus (PubMed:26583432). Plays a role in cell metabolism by regulating adiponecting ans insulin signaling pathways and adaptative thermogenesis (PubMed:24879834) (By similarity). In muscle, negatively regulates adiponectin-simulated glucose uptake and fatty acid oxidation by inhibiting adiponectin signaling pathway through APPL1 sequestration thereby antagonizing APPL1 action (By similarity). In muscles, negativeliy regulates insulin-induced plasma membrane recruitment of GLUT4 and glucose uptake through interaction with TBC1D1 (PubMed:24879834). Plays a role in cold and diet-induced adaptive thermogenesis by activating ventromedial hypothalamus (VMH) neurons throught AMPK inhibition which enhances sympathetic outflow to subcutaneous white adipose tissue (sWAT), sWAT beiging and cold tolerance (By similarity). Also plays a role in other signaling pathways namely Wnt/beta-catenin, HGF and glucocorticoid receptor signaling (PubMed:19433865) (By similarity). Positive regulator of beta-catenin/TCF-dependent transcription through direct interaction with RUVBL2/reptin resulting in the relief of RUVBL2-mediated repression of beta-catenin/TCF target genes by modulating the interactions within the beta-catenin-reptin-HDAC complex (PubMed:19433865). May affect adult neurogenesis in hippocampus and olfactory system via regulating the sensitivity of glucocorticoid receptor. Required for fibroblast migration through HGF cell signaling (By similarity). {ECO:0000250|UniProtKB:Q8K3G9, ECO:0000269|PubMed:15016378, ECO:0000269|PubMed:19433865, ECO:0000269|PubMed:24879834, ECO:0000269|PubMed:26583432}.
Ensembl transtripts involved in fusion geneENST idsENST00000344293, ENST00000474136, 
ENST00000346798, ENST00000348990, 
ENST00000354192, ENST00000357903, 
ENST00000358918, ENST00000359726, 
ENST00000439274, ENST00000440126, 
ENST00000448388, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 6 X 7=46225 X 18 X 10=4500
# samples 1227
** MAII scorelog2(12/462*10)=-1.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(27/4500*10)=-4.05889368905357
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TAF3 [Title/Abstract] AND APP [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TAF3 [Title/Abstract] AND APP [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TAF3(8019286)-APP(27394358), # samples:1
Anticipated loss of major functional domain due to fusion event.TAF3-APP 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.
TAF3-APP 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.
TAF3-APP 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.
TAF3-APP 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
HgeneTAF3

GO:0000122

negative regulation of transcription by RNA polymerase II

18549481

HgeneTAF3

GO:0043433

negative regulation of DNA-binding transcription factor activity

18549481

HgeneTAF3

GO:0051457

maintenance of protein location in nucleus

15870280

TgeneAPP

GO:0001934

positive regulation of protein phosphorylation

11404397

TgeneAPP

GO:0008285

negative regulation of cell proliferation

22944668

TgeneAPP

GO:1905606

regulation of presynapse assembly

19726636



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/chr10:8019286/chr21:27394358)
- 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 TAF3 (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 APP (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)
ENST00000344293TAF3chr108019286-ENST00000346798APPchr2127394358-5292252113741711344
ENST00000344293TAF3chr108019286-ENST00000354192APPchr2127394358-5067252113739461269
ENST00000344293TAF3chr108019286-ENST00000348990APPchr2127394358-5067252113739461269
ENST00000344293TAF3chr108019286-ENST00000357903APPchr2127394358-5235252113741141325
ENST00000344293TAF3chr108019286-ENST00000358918APPchr2127394358-5237252113741171326
ENST00000344293TAF3chr108019286-ENST00000359726APPchr2127394358-5123252113740031288
ENST00000344293TAF3chr108019286-ENST00000448388APPchr2127394358-4290252113739461269
ENST00000344293TAF3chr108019286-ENST00000440126APPchr2127394358-4454252113741141325
ENST00000344293TAF3chr108019286-ENST00000439274APPchr2127394358-4510252113741711344

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
ENST00000344293ENST00000346798TAF3chr108019286-APPchr2127394358-0.0009509060.9990491
ENST00000344293ENST00000354192TAF3chr108019286-APPchr2127394358-0.0006805240.99931943
ENST00000344293ENST00000348990TAF3chr108019286-APPchr2127394358-0.0006805240.99931943
ENST00000344293ENST00000357903TAF3chr108019286-APPchr2127394358-0.0013148390.9986852
ENST00000344293ENST00000358918TAF3chr108019286-APPchr2127394358-0.0010064150.9989936
ENST00000344293ENST00000359726TAF3chr108019286-APPchr2127394358-0.0006271890.9993728
ENST00000344293ENST00000448388TAF3chr108019286-APPchr2127394358-0.0015802790.99841976
ENST00000344293ENST00000440126TAF3chr108019286-APPchr2127394358-0.0026567270.99734324
ENST00000344293ENST00000439274TAF3chr108019286-APPchr2127394358-0.0019952230.99800473

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 TAF3-APP

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TAF3chr108019286APPchr21273943582521795RLTLRVGAGQDKIEDKVVEVAEEEEV

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Potential FusionNeoAntigen Information of TAF3-APP 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.
TAF3-APP_8019286_27394358.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)
TAF3-APPchr108019286chr21273943582521HLA-B41:01IEDKVVEV0.99360.80071220
TAF3-APPchr108019286chr21273943582521HLA-B39:13IEDKVVEV0.94160.90151220
TAF3-APPchr108019286chr21273943582521HLA-B45:01IEDKVVEVA0.99680.74821221
TAF3-APPchr108019286chr21273943582521HLA-B50:02IEDKVVEVA0.99660.55981221
TAF3-APPchr108019286chr21273943582521HLA-A02:60KIEDKVVEV0.98680.66791120
TAF3-APPchr108019286chr21273943582521HLA-A02:24KIEDKVVEV0.98640.66631120
TAF3-APPchr108019286chr21273943582521HLA-A02:67KIEDKVVEV0.98640.66631120
TAF3-APPchr108019286chr21273943582521HLA-A02:30KIEDKVVEV0.98640.66631120
TAF3-APPchr108019286chr21273943582521HLA-A02:38KIEDKVVEV0.98580.59851120
TAF3-APPchr108019286chr21273943582521HLA-A02:21KIEDKVVEV0.98570.76521120
TAF3-APPchr108019286chr21273943582521HLA-A02:11KIEDKVVEV0.98550.68391120
TAF3-APPchr108019286chr21273943582521HLA-A02:04KIEDKVVEV0.98330.65191120
TAF3-APPchr108019286chr21273943582521HLA-A02:27KIEDKVVEV0.97860.6061120
TAF3-APPchr108019286chr21273943582521HLA-A02:13KIEDKVVEV0.97440.67511120
TAF3-APPchr108019286chr21273943582521HLA-A02:16KIEDKVVEV0.96390.51581120
TAF3-APPchr108019286chr21273943582521HLA-A02:35KIEDKVVEV0.87680.70561120
TAF3-APPchr108019286chr21273943582521HLA-A02:29KIEDKVVEV0.85920.66751120
TAF3-APPchr108019286chr21273943582521HLA-B13:02GQDKIEDKV0.84520.8128817
TAF3-APPchr108019286chr21273943582521HLA-A02:20KIEDKVVEV0.83910.66971120
TAF3-APPchr108019286chr21273943582521HLA-B50:01IEDKVVEVA0.73030.72611221
TAF3-APPchr108019286chr21273943582521HLA-B13:01GQDKIEDKV0.68060.9586817
TAF3-APPchr108019286chr21273943582521HLA-B41:01IEDKVVEVA0.6520.84091221
TAF3-APPchr108019286chr21273943582521HLA-B13:02KIEDKVVEV0.39880.54911120
TAF3-APPchr108019286chr21273943582521HLA-B45:01KIEDKVVEVA0.78870.73321121
TAF3-APPchr108019286chr21273943582521HLA-B41:01KIEDKVVEVA0.6590.82341121
TAF3-APPchr108019286chr21273943582521HLA-B40:06IEDKVVEV10.5521220
TAF3-APPchr108019286chr21273943582521HLA-B39:08IEDKVVEV0.99370.73071220
TAF3-APPchr108019286chr21273943582521HLA-C05:09KIEDKVVEV0.99990.93141120
TAF3-APPchr108019286chr21273943582521HLA-C04:10KIEDKVVEV0.99990.73951120
TAF3-APPchr108019286chr21273943582521HLA-C04:07KIEDKVVEV0.99980.73371120
TAF3-APPchr108019286chr21273943582521HLA-C08:15KIEDKVVEV0.99930.97371120
TAF3-APPchr108019286chr21273943582521HLA-B40:06IEDKVVEVA0.99880.54491221
TAF3-APPchr108019286chr21273943582521HLA-C15:06KIEDKVVEV0.99730.92291120
TAF3-APPchr108019286chr21273943582521HLA-C04:06KIEDKVVEV0.99590.92141120
TAF3-APPchr108019286chr21273943582521HLA-A02:07KIEDKVVEV0.98690.70741120
TAF3-APPchr108019286chr21273943582521HLA-A02:01KIEDKVVEV0.98640.66631120
TAF3-APPchr108019286chr21273943582521HLA-C04:14KIEDKVVEV0.9520.83181120
TAF3-APPchr108019286chr21273943582521HLA-C08:04KIEDKVVEV0.83310.95661120
TAF3-APPchr108019286chr21273943582521HLA-C08:13KIEDKVVEV0.83310.95661120
TAF3-APPchr108019286chr21273943582521HLA-C02:06KIEDKVVEV0.73250.95271120
TAF3-APPchr108019286chr21273943582521HLA-C08:03KIEDKVVEV0.45890.97941120
TAF3-APPchr108019286chr21273943582521HLA-B39:08GQDKIEDKV0.2690.8663817
TAF3-APPchr108019286chr21273943582521HLA-B40:04IEDKVVEV0.99970.73941220
TAF3-APPchr108019286chr21273943582521HLA-B41:03IEDKVVEV0.99230.55241220
TAF3-APPchr108019286chr21273943582521HLA-C04:03KIEDKVVEV0.99990.74451120
TAF3-APPchr108019286chr21273943582521HLA-C05:01KIEDKVVEV0.99990.93141120
TAF3-APPchr108019286chr21273943582521HLA-C18:01KIEDKVVEV0.99990.72941120
TAF3-APPchr108019286chr21273943582521HLA-C04:01KIEDKVVEV0.99980.73371120
TAF3-APPchr108019286chr21273943582521HLA-C08:02KIEDKVVEV0.99930.97371120
TAF3-APPchr108019286chr21273943582521HLA-C01:03KIEDKVVEV0.99890.91651120
TAF3-APPchr108019286chr21273943582521HLA-C15:02KIEDKVVEV0.99870.91661120
TAF3-APPchr108019286chr21273943582521HLA-C15:05KIEDKVVEV0.99820.94351120
TAF3-APPchr108019286chr21273943582521HLA-A02:03KIEDKVVEV0.98620.66381120
TAF3-APPchr108019286chr21273943582521HLA-A02:14KIEDKVVEV0.98620.60991120
TAF3-APPchr108019286chr21273943582521HLA-A02:06KIEDKVVEV0.98570.76521120
TAF3-APPchr108019286chr21273943582521HLA-C04:04KIEDKVVEV0.98340.92711120
TAF3-APPchr108019286chr21273943582521HLA-B40:04IEDKVVEVA0.98040.73421221
TAF3-APPchr108019286chr21273943582521HLA-C17:01KIEDKVVEV0.74880.87361120
TAF3-APPchr108019286chr21273943582521HLA-B50:04IEDKVVEVA0.73030.72611221
TAF3-APPchr108019286chr21273943582521HLA-B50:05IEDKVVEVA0.73030.72611221
TAF3-APPchr108019286chr21273943582521HLA-B41:03IEDKVVEVA0.72750.62761221
TAF3-APPchr108019286chr21273943582521HLA-C08:01KIEDKVVEV0.45890.97941120
TAF3-APPchr108019286chr21273943582521HLA-C07:04KIEDKVVEV0.34760.94341120
TAF3-APPchr108019286chr21273943582521HLA-B07:13KIEDKVVEV0.18720.72851120

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Potential FusionNeoAntigen Information of TAF3-APP 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 TAF3-APP

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
2651GAGQDKIEDKVVEVTAF3APPchr108019286chr21273943582521

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TAF3-APP

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-B14:023BVN2651GAGQDKIEDKVVEV-7.15543-7.26883
HLA-B14:023BVN2651GAGQDKIEDKVVEV-4.77435-5.80965
HLA-B52:013W392651GAGQDKIEDKVVEV-6.80875-6.92215
HLA-B52:013W392651GAGQDKIEDKVVEV-4.20386-5.23916
HLA-A11:014UQ22651GAGQDKIEDKVVEV-7.5194-8.5547
HLA-A11:014UQ22651GAGQDKIEDKVVEV-6.9601-7.0735
HLA-A24:025HGA2651GAGQDKIEDKVVEV-7.52403-7.63743
HLA-A24:025HGA2651GAGQDKIEDKVVEV-5.82433-6.85963
HLA-B27:056PYJ2651GAGQDKIEDKVVEV-3.28285-4.31815
HLA-B44:053DX82651GAGQDKIEDKVVEV-5.91172-6.94702
HLA-B44:053DX82651GAGQDKIEDKVVEV-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of TAF3-APP

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
TAF3-APPchr108019286chr21273943581120KIEDKVVEVCAAGATTGAAGACAAAGTAGTAGAAGT
TAF3-APPchr108019286chr21273943581121KIEDKVVEVACAAGATTGAAGACAAAGTAGTAGAAGTAGC
TAF3-APPchr108019286chr21273943581220IEDKVVEVGATTGAAGACAAAGTAGTAGAAGT
TAF3-APPchr108019286chr21273943581221IEDKVVEVAGATTGAAGACAAAGTAGTAGAAGTAGC
TAF3-APPchr108019286chr2127394358817GQDKIEDKVTGGCCAAGACAAGATTGAAGACAAAGT

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 TAF3-APP

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
BLCATAF3-APPchr108019286ENST00000344293chr2127394358ENST00000346798TCGA-4Z-AA87-01A

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Potential target of CAR-T therapy development for TAF3-APP

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
TgeneAPPchr10:8019286chr21:27394358ENST00000346798418702_7220771.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000348990416702_7220696.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000354192315702_7220640.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000357903417702_7220752.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000358918417702_7220753.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000359726417702_7220715.0TransmembraneHelical
TgeneAPPchr10:8019286chr21:27394358ENST00000440126417702_7220747.0TransmembraneHelical

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 TAF3-APP

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 TAF3-APP

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