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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:ARID1B-SASH1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARID1B-SASH1
FusionPDB ID: 6418
FusionGDB2.0 ID: 6418
HgeneTgene
Gene symbol

ARID1B

SASH1

Gene ID

57492

23328

Gene nameAT-rich interaction domain 1BSAM and SH3 domain containing 1
Synonyms6A3-5|BAF250B|BRIGHT|CSS1|DAN15|ELD/OSA1|MRD12|OSA2|P250RCAPOK|DUH1|SH3D6A|dJ323M4.1
Cytomap

6q25.3

6q24.3-q25.1

Type of geneprotein-codingprotein-coding
DescriptionAT-rich interactive domain-containing protein 1BARID domain-containing protein 1BAT rich interactive domain 1B (SWI1-like)BRG1-associated factor 250bBRG1-binding protein ELD/OSA1ELD (eyelid)/OSA proteinSAM and SH3 domain-containing protein 1proline-glutamate repeat-containing protein
Modification date2020032020200313
UniProtAcc

Q8NFD5

Main function of 5'-partner protein: FUNCTION: Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). Binds DNA non-specifically (PubMed:14982958, PubMed:15170388). {ECO:0000250|UniProtKB:E9Q4N7, ECO:0000269|PubMed:14982958, ECO:0000269|PubMed:15170388, ECO:0000303|PubMed:12672490, ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}.

O94885

Main function of 5'-partner protein: FUNCTION: Is a positive regulator of NF-kappa-B signaling downstream of TLR4 activation. It acts as a scaffold molecule to assemble a molecular complex that includes TRAF6, MAP3K7, CHUK and IKBKB, thereby facilitating NF-kappa-B signaling activation (PubMed:23776175). Regulates TRAF6 and MAP3K7 ubiquitination (PubMed:23776175). Involved in the regulation of cell mobility (PubMed:23333244, PubMed:23776175, PubMed:25315659). Regulates lipolysaccharide (LPS)-induced endothelial cell migration (PubMed:23776175). Is involved in the regulation of skin pigmentation through the control of melanocyte migration in the epidermis (PubMed:23333244). {ECO:0000269|PubMed:23333244, ECO:0000269|PubMed:23776175, ECO:0000269|PubMed:25315659}.
Ensembl transtripts involved in fusion geneENST idsENST00000275248, ENST00000346085, 
ENST00000350026, ENST00000367148, 
ENST00000478761, 
ENST00000470750, 
ENST00000367467, ENST00000367469, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score27 X 18 X 14=680410 X 8 X 7=560
# samples 3112
** MAII scorelog2(31/6804*10)=-4.45604302038915
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/560*10)=-2.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ARID1B [Title/Abstract] AND SASH1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARID1B [Title/Abstract] AND SASH1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SASH1(148711398)-ARID1B(157256600), # samples:3
ARID1B(157150555)-SASH1(148711270), # samples:2
Anticipated loss of major functional domain due to fusion event.ARID1B-SASH1 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.
ARID1B-SASH1 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.
ARID1B-SASH1 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.
ARID1B-SASH1 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.
SASH1-ARID1B 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.
SASH1-ARID1B 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
TgeneSASH1

GO:0000209

protein polyubiquitination

23776175

TgeneSASH1

GO:0010595

positive regulation of endothelial cell migration

23776175

TgeneSASH1

GO:1900044

regulation of protein K63-linked ubiquitination

23776175

TgeneSASH1

GO:1902498

regulation of protein autoubiquitination

23776175



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/chr6:148711398/chr6:157256600)
- 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 ARID1B (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 SASH1 (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)
ENST00000350026ARID1Bchr6157150555+ENST00000367469SASH1chr6148711270+2255173811971656
ENST00000350026ARID1Bchr6157150555+ENST00000367467SASH1chr6148711270+88181738153251774
ENST00000346085ARID1Bchr6157150555+ENST00000367469SASH1chr6148711270+2255173811971656
ENST00000346085ARID1Bchr6157150555+ENST00000367467SASH1chr6148711270+88181738153251774
ENST00000367148ARID1Bchr6157150555+ENST00000367469SASH1chr6148711270+2254173701970656
ENST00000367148ARID1Bchr6157150555+ENST00000367467SASH1chr6148711270+88171737053241774
ENST00000275248ARID1Bchr6157150555+ENST00000367469SASH1chr6148711270+22321715771948623
ENST00000275248ARID1Bchr6157150555+ENST00000367467SASH1chr6148711270+879517157753021741

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
ENST00000350026ENST00000367469ARID1Bchr6157150555+SASH1chr6148711270+0.0137830050.986217
ENST00000350026ENST00000367467ARID1Bchr6157150555+SASH1chr6148711270+0.0009849370.9990151
ENST00000346085ENST00000367469ARID1Bchr6157150555+SASH1chr6148711270+0.0137830050.986217
ENST00000346085ENST00000367467ARID1Bchr6157150555+SASH1chr6148711270+0.0009849370.9990151
ENST00000367148ENST00000367469ARID1Bchr6157150555+SASH1chr6148711270+0.0139642420.9860357
ENST00000367148ENST00000367467ARID1Bchr6157150555+SASH1chr6148711270+0.000981610.99901843
ENST00000275248ENST00000367469ARID1Bchr6157150555+SASH1chr6148711270+0.0117705740.9882294
ENST00000275248ENST00000367467ARID1Bchr6157150555+SASH1chr6148711270+0.0011428230.99885714

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 ARID1B-SASH1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARID1Bchr6157150555SASH1chr61487112701715545TPGAMAGMQYPQQQDGSLGNIDDLAQ
ARID1Bchr6157150555SASH1chr61487112701737578TPGAMAGMQYPQQQDGSLGNIDDLAQ
ARID1Bchr6157150555SASH1chr61487112701738578TPGAMAGMQYPQQQDGSLGNIDDLAQ

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Potential FusionNeoAntigen Information of ARID1B-SASH1 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.
ARID1B-SASH1_157150555_148711270.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)
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:01YPQQQDGSL0.97260.9258918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:03YPQQQDGSL0.96670.9239918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:08YPQQQDGSL0.96340.9123918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:05YPQQQDGSL0.90420.7787918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:02YPQQQDGSL0.87210.9663918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:04YPQQQDGSL0.87210.9663918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B53:01YPQQQDGSL0.87140.534918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:01YPQQQDGSL0.72370.9526918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B81:01YPQQQDGSL0.3220.6476918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B82:01YPQQQDGSL0.09530.6053918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B13:02QQQDGSLGNI0.35750.80361121
ARID1B-SASH1chr6157150555chr61487112701715HLA-B48:01MQYPQQQDGSL0.98910.8116718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:13MQYPQQQDGSL0.9650.9721718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B13:01MQYPQQQDGSL0.95360.9932718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B13:02MQYPQQQDGSL0.93380.7583718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:03MQYPQQQDGSL0.90360.9519718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B52:01MQYPQQQDGSL0.660.987718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B07:12YPQQQDGSL0.92230.6169918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B14:03YPQQQDGSL0.89760.8646918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B56:04YPQQQDGSL0.87380.5577918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:12YPQQQDGSL0.87210.9663918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:09YPQQQDGSL0.7910.8543918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:10YPQQQDGSL0.75350.961918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B78:01YPQQQDGSL0.50730.5987918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B42:02YPQQQDGSL0.42980.8072918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B42:01YPQQQDGSL0.35870.8026918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B07:12QYPQQQDGSL0.55990.6316818
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:04MQYPQQQDGSL0.99910.9551718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:07MQYPQQQDGSL0.99910.8326718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B48:03MQYPQQQDGSL0.98490.5758718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B07:09YPQQQDGSL0.97610.5175918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:23YPQQQDGSL0.97390.9322918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:77YPQQQDGSL0.97260.9258918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:13YPQQQDGSL0.96350.9285918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:11YPQQQDGSL0.91340.92918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:22YPQQQDGSL0.90980.5536918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:30YPQQQDGSL0.90640.8494918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:17YPQQQDGSL0.90640.8494918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B56:02YPQQQDGSL0.87380.5577918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:09YPQQQDGSL0.87210.9663918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B55:04YPQQQDGSL0.87080.5776918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:24YPQQQDGSL0.83860.9406918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B67:01YPQQQDGSL0.77610.9571918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:11YPQQQDGSL0.59510.9379918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:09YPQQQDGSL0.58710.7492918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B78:02YPQQQDGSL0.53590.6958918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B08:12YPQQQDGSL0.38430.8658918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B35:43YPQQQDGSL0.12310.8977918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:08YPQQQDGSL0.09630.8916918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B82:02YPQQQDGSL0.09530.6053918
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:68MQYPQQQDGSL0.99970.7932718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:24MQYPQQQDGSL0.99960.9485718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:53MQYPQQQDGSL0.99920.9174718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:73MQYPQQQDGSL0.99830.8968718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B15:30MQYPQQQDGSL0.99730.9442718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B40:12MQYPQQQDGSL0.98490.5758718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B39:02MQYPQQQDGSL0.97540.9738718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B40:49MQYPQQQDGSL0.97110.5305718
ARID1B-SASH1chr6157150555chr61487112701715HLA-B40:21MQYPQQQDGSL0.96740.7035718

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Potential FusionNeoAntigen Information of ARID1B-SASH1 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 ARID1B-SASH1

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
2984GMQYPQQQDGSLGNARID1BSASH1chr6157150555chr61487112701715

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARID1B-SASH1

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-B14:023BVN2984GMQYPQQQDGSLGN-8.05428-8.16608
HLA-B14:023BVN2984GMQYPQQQDGSLGN-6.23096-7.27406
HLA-B52:013W392984GMQYPQQQDGSLGN-7.47361-7.58541
HLA-B52:013W392984GMQYPQQQDGSLGN-5.13706-6.18016
HLA-A11:014UQ22984GMQYPQQQDGSLGN-7.22203-7.33383
HLA-A11:014UQ22984GMQYPQQQDGSLGN-7.19046-8.23356
HLA-A24:025HGA2984GMQYPQQQDGSLGN-8.7776-9.8207
HLA-A24:025HGA2984GMQYPQQQDGSLGN-6.19371-6.30551
HLA-B44:053DX82984GMQYPQQQDGSLGN-6.55017-6.66197
HLA-B44:053DX82984GMQYPQQQDGSLGN-3.82918-4.87228
HLA-A02:016TDR2984GMQYPQQQDGSLGN-6.8339-6.9457
HLA-A02:016TDR2984GMQYPQQQDGSLGN-0.262577-1.30568

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Vaccine Design for the FusionNeoAntigens of ARID1B-SASH1

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
ARID1B-SASH1chr6157150555chr61487112701121QQQDGSLGNICAGCAGGACGGTTCACTGGGAAACATCGAT
ARID1B-SASH1chr6157150555chr6148711270718MQYPQQQDGSLCAGTACCCTCAGCAGCAGGACGGTTCACTGGGA
ARID1B-SASH1chr6157150555chr6148711270818QYPQQQDGSLTACCCTCAGCAGCAGGACGGTTCACTGGGA
ARID1B-SASH1chr6157150555chr6148711270918YPQQQDGSLCCTCAGCAGCAGGACGGTTCACTGGGA

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 ARID1B-SASH1

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
SKCMARID1B-SASH1chr6157150555ENST00000275248chr6148711270ENST00000367467TCGA-ER-A197-06A

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Potential target of CAR-T therapy development for ARID1B-SASH1

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 ARID1B-SASH1

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 ARID1B-SASH1

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
TgeneSASH1C2675711Dyschromatosis Universalis Hereditaria 16CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneSASH1C3492944Lentiginosis Profusa1ORPHANET