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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:PTCH1-TPM1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PTCH1-TPM1
FusionPDB ID: 69869
FusionGDB2.0 ID: 69869
HgeneTgene
Gene symbol

PTCH1

TPM1

Gene ID

5727

7168

Gene namepatched 1tropomyosin 1
SynonymsBCNS|NBCCS|PTC|PTC1|PTCHC15orf13|CMD1Y|CMH3|HEL-S-265|HTM-alpha|LVNC9|TMSA
Cytomap

9q22.32

15q22.2

Type of geneprotein-codingprotein-coding
Descriptionprotein patched homolog 1tropomyosin alpha-1 chaincardiomyopathy, hypertrophic 3epididymis secretory protein Li 265sarcomeric tropomyosin kappa
Modification date2020031420200320
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000331920, ENST00000375274, 
ENST00000418258, ENST00000421141, 
ENST00000429896, ENST00000430669, 
ENST00000437951, ENST00000468211, 
ENST00000548379, 
ENST00000267996, 
ENST00000317516, ENST00000334895, 
ENST00000357980, ENST00000403994, 
ENST00000404484, ENST00000559281, 
ENST00000559397, ENST00000559556, 
ENST00000560445, ENST00000560959, 
ENST00000288398, ENST00000358278, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 7 X 4=16814 X 8 X 8=896
# samples 716
** MAII scorelog2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/896*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PTCH1 [Title/Abstract] AND TPM1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PTCH1 [Title/Abstract] AND TPM1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PTCH1(98224138)-TPM1(63349184), # samples:1
Anticipated loss of major functional domain due to fusion event.PTCH1-TPM1 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.
PTCH1-TPM1 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.
PTCH1-TPM1 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.
PTCH1-TPM1 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.
PTCH1-TPM1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
PTCH1-TPM1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor 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
HgenePTCH1

GO:0010875

positive regulation of cholesterol efflux

21931618

HgenePTCH1

GO:0072659

protein localization to plasma membrane

11278759



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/chr9:98224138/chr15:63349184)
- 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 PTCH1 (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 TPM1 (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)
ENST00000418258PTCH1chr998224138-ENST00000288398TPM1chr1563349184+3622276511333791088
ENST00000418258PTCH1chr998224138-ENST00000358278TPM1chr1563349184+4097276511333791088
ENST00000430669PTCH1chr998224138-ENST00000288398TPM1chr1563349184+3948309158637051039
ENST00000430669PTCH1chr998224138-ENST00000358278TPM1chr1563349184+4423309158637051039

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
ENST00000418258ENST00000288398PTCH1chr998224138-TPM1chr1563349184+0.0016434650.9983565
ENST00000418258ENST00000358278PTCH1chr998224138-TPM1chr1563349184+0.0011510030.99884903
ENST00000430669ENST00000288398PTCH1chr998224138-TPM1chr1563349184+0.0010952710.9989047
ENST00000430669ENST00000358278PTCH1chr998224138-TPM1chr1563349184+0.0007610520.99923897

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 PTCH1-TPM1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PTCH1chr998224138TPM1chr15633491842765884QTGSRDKPIDISQAEADVASLNRRIQ
PTCH1chr998224138TPM1chr15633491843091835QTGSRDKPIDISQAEADVASLNRRIQ

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Potential FusionNeoAntigen Information of PTCH1-TPM1 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.
PTCH1-TPM1_98224138_63349184.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)
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:03QAEADVASL0.69970.8761221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:04QAEADVASL0.52250.9821221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:02QAEADVASL0.52250.9821221
PTCH1-TPM1chr998224138chr15633491842765HLA-B48:01SQAEADVASL0.98630.62641121
PTCH1-TPM1chr998224138chr15633491842765HLA-B39:13SQAEADVASL0.95210.90831121
PTCH1-TPM1chr998224138chr15633491842765HLA-A02:21SQAEADVASL0.91260.73751121
PTCH1-TPM1chr998224138chr15633491842765HLA-B13:02SQAEADVASL0.83450.65681121
PTCH1-TPM1chr998224138chr15633491842765HLA-B13:01SQAEADVASL0.82010.97111121
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:15QAEADVASL0.99960.96911221
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:04QAEADVASL0.95190.97371221
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:13QAEADVASL0.95190.97371221
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:03QAEADVASL0.83360.98361221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:12QAEADVASL0.52250.9821221
PTCH1-TPM1chr998224138chr15633491842765HLA-B39:08SQAEADVASL0.97950.87691121
PTCH1-TPM1chr998224138chr15633491842765HLA-B54:01KPIDISQAEA0.96850.5095616
PTCH1-TPM1chr998224138chr15633491842765HLA-B48:03SQAEADVASL0.96590.51911121
PTCH1-TPM1chr998224138chr15633491842765HLA-B39:05SQAEADVASL0.94260.93231121
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:02QAEADVASL0.99960.96911221
PTCH1-TPM1chr998224138chr15633491842765HLA-C03:06QAEADVASL0.93380.99331221
PTCH1-TPM1chr998224138chr15633491842765HLA-C08:01QAEADVASL0.83360.98361221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:13QAEADVASL0.67710.88011221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:09QAEADVASL0.52250.9821221
PTCH1-TPM1chr998224138chr15633491842765HLA-B35:22QAEADVASL0.39180.5031221
PTCH1-TPM1chr998224138chr15633491842765HLA-B15:73SQAEADVASL0.99730.88461121
PTCH1-TPM1chr998224138chr15633491842765HLA-B15:30SQAEADVASL0.99430.82161121
PTCH1-TPM1chr998224138chr15633491842765HLA-B39:02SQAEADVASL0.97670.91161121
PTCH1-TPM1chr998224138chr15633491842765HLA-B39:11SQAEADVASL0.97040.87581121
PTCH1-TPM1chr998224138chr15633491842765HLA-B40:12SQAEADVASL0.96590.51911121
PTCH1-TPM1chr998224138chr15633491842765HLA-A02:14SQAEADVASL0.91570.59761121
PTCH1-TPM1chr998224138chr15633491842765HLA-A02:06SQAEADVASL0.91260.73751121
PTCH1-TPM1chr998224138chr15633491842765HLA-B40:21SQAEADVASL0.88380.55491121
PTCH1-TPM1chr998224138chr15633491842765HLA-B56:05KPIDISQAEA0.77560.5272616

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Potential FusionNeoAntigen Information of PTCH1-TPM1 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.
PTCH1-TPM1_98224138_63349184.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)
PTCH1-TPM1chr998224138chr15633491842765DRB1-0467DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB1-0904DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB1-0906DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB1-0906RDKPIDISQAEADVA419
PTCH1-TPM1chr998224138chr15633491842765DRB1-0908DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB1-0908RDKPIDISQAEADVA419
PTCH1-TPM1chr998224138chr15633491842765DRB1-1410DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0101PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0101KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0101DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0103PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0103KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0103DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0104PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0104KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0104DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0106PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0106KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0106DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0107PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0107KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0107DKPIDISQAEADVAS520
PTCH1-TPM1chr998224138chr15633491842765DRB4-0108PIDISQAEADVASLN722
PTCH1-TPM1chr998224138chr15633491842765DRB4-0108KPIDISQAEADVASL621
PTCH1-TPM1chr998224138chr15633491842765DRB4-0108DKPIDISQAEADVAS520

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Fusion breakpoint peptide structures of PTCH1-TPM1

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
4481KPIDISQAEADVASPTCH1TPM1chr998224138chr15633491842765

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PTCH1-TPM1

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-B14:023BVN4481KPIDISQAEADVAS-7.9962-8.1096
HLA-B14:023BVN4481KPIDISQAEADVAS-5.70842-6.74372
HLA-B52:013W394481KPIDISQAEADVAS-6.83737-6.95077
HLA-B52:013W394481KPIDISQAEADVAS-4.4836-5.5189
HLA-A11:014UQ24481KPIDISQAEADVAS-10.0067-10.1201
HLA-A11:014UQ24481KPIDISQAEADVAS-9.03915-10.0745
HLA-A24:025HGA4481KPIDISQAEADVAS-6.56204-6.67544
HLA-A24:025HGA4481KPIDISQAEADVAS-5.42271-6.45801
HLA-B44:053DX84481KPIDISQAEADVAS-7.85648-8.89178
HLA-B44:053DX84481KPIDISQAEADVAS-5.3978-5.5112
HLA-A02:016TDR4481KPIDISQAEADVAS-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PTCH1-TPM1

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
PTCH1-TPM1chr998224138chr15633491841121SQAEADVASLAGCCAGGCTGAAGCCGACGTAGCTTCTCTG
PTCH1-TPM1chr998224138chr15633491841221QAEADVASLCAGGCTGAAGCCGACGTAGCTTCTCTG
PTCH1-TPM1chr998224138chr1563349184616KPIDISQAEAAAGCCCATCGACATCAGCCAGGCTGAAGCC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PTCH1-TPM1chr998224138chr1563349184419RDKPIDISQAEADVACGCGATAAGCCCATCGACATCAGCCAGGCTGAAGCCGACGTAGCT
PTCH1-TPM1chr998224138chr1563349184520DKPIDISQAEADVASGATAAGCCCATCGACATCAGCCAGGCTGAAGCCGACGTAGCTTCT
PTCH1-TPM1chr998224138chr1563349184621KPIDISQAEADVASLAAGCCCATCGACATCAGCCAGGCTGAAGCCGACGTAGCTTCTCTG
PTCH1-TPM1chr998224138chr1563349184722PIDISQAEADVASLNCCCATCGACATCAGCCAGGCTGAAGCCGACGTAGCTTCTCTGAAC

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Information of the samples that have these potential fusion neoantigens of PTCH1-TPM1

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
SARCPTCH1-TPM1chr998224138ENST00000418258chr1563349184ENST00000288398TCGA-DX-A6B9-01A

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Potential target of CAR-T therapy development for PTCH1-TPM1

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
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624101_1219012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624437_4579012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624473_4939012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624502_5229012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624548_5689012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624578_5989012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000331920-1624749_7699012534.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624101_1219001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624437_4579001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624473_4939001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624502_5229001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624548_5689001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624578_5989001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000375274-1624749_7699001526.3333333333333TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624101_1217502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624437_4577502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624473_4937502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624502_5227502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624548_5687502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000418258-1624578_5987502461.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624101_1217502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624437_4577502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624473_4937502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624502_5227502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624548_5687502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000421141-1624578_5987502513.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624101_1217502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624437_4577502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624473_4937502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624502_5227502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624548_5687502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000429896-1624578_5987502093.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623101_1218351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623437_4578351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623473_4938351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623502_5228351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623548_5688351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623578_5988351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000430669-1623749_7698351382.0TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624101_1218352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624437_4578352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624473_4938352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624502_5228352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624548_5688352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624578_5988352468.3333333333335TransmembraneHelical
HgenePTCH1chr9:98224138chr15:63349184ENST00000437951-1624749_7698352468.3333333333335TransmembraneHelical

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 PTCH1-TPM1

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 PTCH1-TPM1

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