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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:ATF1-HP1BP3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATF1-HP1BP3
FusionPDB ID: 7403
FusionGDB2.0 ID: 7403
HgeneTgene
Gene symbol

ATF1

HP1BP3

Gene ID

2668

50809

Gene nameglial cell derived neurotrophic factorheterochromatin protein 1 binding protein 3
SynonymsATF|ATF1|ATF2|HFB1-GDNF|HSCR3HP1-BP74|HP1BP74
Cytomap

5p13.2

1p36.12

Type of geneprotein-codingprotein-coding
Descriptionglial cell line-derived neurotrophic factorastrocyte-derived trophic factorheterochromatin protein 1-binding protein 3
Modification date2020031420200313
UniProtAcc

P18846

Main function of 5'-partner protein: FUNCTION: This protein binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), a sequence present in many viral and cellular promoters. Binds to the Tax-responsive element (TRE) of HTLV-I. Mediates PKA-induced stimulation of CRE-reporter genes. Represses the expression of FTH1 and other antioxidant detoxification genes. Triggers cell proliferation and transformation. {ECO:0000269|PubMed:18794154, ECO:0000269|PubMed:20980392}.

Q5SSJ5

Main function of 5'-partner protein: FUNCTION: Component of heterochromatin that maintains heterochromatin integrity during G1/S progression and regulates the duration of G1 phase to critically influence cell proliferative capacity (PubMed:24830416). Mediates chromatin condensation during hypoxia, leading to increased tumor cell viability, radio-resistance, chemo-resistance and self-renewal(PubMed:25100860). {ECO:0000269|PubMed:24830416, ECO:0000269|PubMed:25100860}.
Ensembl transtripts involved in fusion geneENST idsENST00000262053, ENST00000539132, 
ENST00000375003, ENST00000375000, 
ENST00000487117, ENST00000312239, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 7 X 6=33622 X 14 X 10=3080
# samples 724
** MAII scorelog2(7/336*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(24/3080*10)=-3.68182403997374
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ATF1 [Title/Abstract] AND HP1BP3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATF1 [Title/Abstract] AND HP1BP3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATF1(51208222)-HP1BP3(21100103), # samples:1
Anticipated loss of major functional domain due to fusion event.ATF1-HP1BP3 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.
ATF1-HP1BP3 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.
ATF1-HP1BP3 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.
ATF1-HP1BP3 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
HgeneATF1

GO:0001755

neural crest cell migration

15242795

HgeneATF1

GO:0008284

positive regulation of cell proliferation

22897442

HgeneATF1

GO:0031175

neuron projection development

15242795

HgeneATF1

GO:0032770

positive regulation of monooxygenase activity

12358785

HgeneATF1

GO:0043524

negative regulation of neuron apoptotic process

8493557

HgeneATF1

GO:0045944

positive regulation of transcription by RNA polymerase II

12358785

HgeneATF1

GO:0048255

mRNA stabilization

12358785

HgeneATF1

GO:0051584

regulation of dopamine uptake involved in synaptic transmission

8493557

HgeneATF1

GO:0072107

positive regulation of ureteric bud formation

8657307

HgeneATF1

GO:0090190

positive regulation of branching involved in ureteric bud morphogenesis

8657307|17229286

HgeneATF1

GO:2001240

negative regulation of extrinsic apoptotic signaling pathway in absence of ligand

10921886

TgeneHP1BP3

GO:0071456

cellular response to hypoxia

25100860



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/chr12:51208222/chr1:21100103)
- 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 ATF1 (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 HP1BP3 (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)
ENST00000262053ATF1chr1251208222+ENST00000312239HP1BP3chr121100103-4141693162004662
ENST00000539132ATF1chr1251208222+ENST00000312239HP1BP3chr121100103-40425942801905541

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
ENST00000262053ENST00000312239ATF1chr1251208222+HP1BP3chr121100103-0.000377190.9996228
ENST00000539132ENST00000312239ATF1chr1251208222+HP1BP3chr121100103-0.0005021370.9994979

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 ATF1-HP1BP3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATF1chr1251208222HP1BP3chr121100103594104DPQLKREIRLMKNSEKDQSKEKEKKV
ATF1chr1251208222HP1BP3chr121100103693225DPQLKREIRLMKNSEKDQSKEKEKKV

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Potential FusionNeoAntigen Information of ATF1-HP1BP3 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.
ATF1-HP1BP3_51208222_21100103.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)
ATF1-HP1BP3chr1251208222chr121100103693HLA-B27:14IRLMKNSEK0.99530.6767716

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Potential FusionNeoAntigen Information of ATF1-HP1BP3 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.
ATF1-HP1BP3_51208222_21100103.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)
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0415KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0415LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0436KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0436LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0437KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0437LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0442KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0442LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0444KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0444LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0453KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0458KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0459KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0459LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0473KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-0473LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1204KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1204LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1209KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1209LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1406KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1406LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1420KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1420LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1429KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1429LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1446KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1446LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1452KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1452LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1452QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1483KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB1-1483LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0101KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0101LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0101QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0101REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0102KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0102LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0102QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0102REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0103KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0103LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0104KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0104LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0105KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0105LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0105QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0105REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0106KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0106LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0106QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0106REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0108NKREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0108NLKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0108NQLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0108NREIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0111KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0111LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0113KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0113LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0113QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0113REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0114KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0114LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0114QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0114REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0202KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0202LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0202QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0202REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0203KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0203LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0204KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0204LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0204QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0204REIRLMKNSEKDQSK520
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0205KREIRLMKNSEKDQS419
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0205LKREIRLMKNSEKDQ318
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0205QLKREIRLMKNSEKD217
ATF1-HP1BP3chr1251208222chr121100103693DRB5-0205REIRLMKNSEKDQSK520

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Fusion breakpoint peptide structures of ATF1-HP1BP3

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
1808EIRLMKNSEKDQSKATF1HP1BP3chr1251208222chr121100103693

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATF1-HP1BP3

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-B14:023BVN1808EIRLMKNSEKDQSK-7.9962-8.1096
HLA-B14:023BVN1808EIRLMKNSEKDQSK-5.70842-6.74372
HLA-B52:013W391808EIRLMKNSEKDQSK-6.83737-6.95077
HLA-B52:013W391808EIRLMKNSEKDQSK-4.4836-5.5189
HLA-A11:014UQ21808EIRLMKNSEKDQSK-10.0067-10.1201
HLA-A11:014UQ21808EIRLMKNSEKDQSK-9.03915-10.0745
HLA-A24:025HGA1808EIRLMKNSEKDQSK-6.56204-6.67544
HLA-A24:025HGA1808EIRLMKNSEKDQSK-5.42271-6.45801
HLA-B44:053DX81808EIRLMKNSEKDQSK-7.85648-8.89178
HLA-B44:053DX81808EIRLMKNSEKDQSK-5.3978-5.5112
HLA-A02:016TDR1808EIRLMKNSEKDQSK-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of ATF1-HP1BP3

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
ATF1-HP1BP3chr1251208222chr121100103716IRLMKNSEKAAGGTTAATGAAAAACAGTGAGAAAGA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ATF1-HP1BP3chr1251208222chr121100103217QLKREIRLMKNSEKDATTGAAAAGAGAAATAAGGTTAATGAAAAACAGTGAGAAAGATCA
ATF1-HP1BP3chr1251208222chr121100103318LKREIRLMKNSEKDQGAAAAGAGAAATAAGGTTAATGAAAAACAGTGAGAAAGATCAGTC
ATF1-HP1BP3chr1251208222chr121100103419KREIRLMKNSEKDQSAAGAGAAATAAGGTTAATGAAAAACAGTGAGAAAGATCAGTCTAA
ATF1-HP1BP3chr1251208222chr121100103520REIRLMKNSEKDQSKAGAAATAAGGTTAATGAAAAACAGTGAGAAAGATCAGTCTAAAGA

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Information of the samples that have these potential fusion neoantigens of ATF1-HP1BP3

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
BRCAATF1-HP1BP3chr1251208222ENST00000262053chr121100103ENST00000312239TCGA-A2-A0T5-01A

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Potential target of CAR-T therapy development for ATF1-HP1BP3

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 ATF1-HP1BP3

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 ATF1-HP1BP3

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
HgeneATF1C0032460Polycystic Ovary Syndrome1CTD_human
HgeneATF1C0206651Clear Cell Sarcoma of Soft Tissue1ORPHANET
HgeneATF1C1136382Sclerocystic Ovaries1CTD_human