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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:BLNK-ZNF536

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BLNK-ZNF536
FusionPDB ID: 9815
FusionGDB2.0 ID: 9815
HgeneTgene
Gene symbol

BLNK

ZNF536

Gene ID

29760

9745

Gene nameB cell linkerzinc finger protein 536
SynonymsAGM4|BASH|BLNK-S|LY57|SLP-65|SLP65|bca-
Cytomap

10q24.1

19q12

Type of geneprotein-codingprotein-coding
DescriptionB-cell linker proteinB cell adaptor containing SH2 domainB-cell activationB-cell adapter containing a SH2 domain proteinB-cell adapter containing a Src homology 2 domain proteinSrc homology 2 domain-containing leukocyte protein of 65 kDaSrc homologyzinc finger protein 536
Modification date2020031320200313
UniProtAcc

Q8WV28

Main function of 5'-partner protein: FUNCTION: Functions as a central linker protein, downstream of the B-cell receptor (BCR), bridging the SYK kinase to a multitude of signaling pathways and regulating biological outcomes of B-cell function and development. Plays a role in the activation of ERK/EPHB2, MAP kinase p38 and JNK. Modulates AP1 activation. Important for the activation of NF-kappa-B and NFAT. Plays an important role in BCR-mediated PLCG1 and PLCG2 activation and Ca(2+) mobilization and is required for trafficking of the BCR to late endosomes. However, does not seem to be required for pre-BCR-mediated activation of MAP kinase and phosphatidyl-inositol 3 (PI3) kinase signaling. May be required for the RAC1-JNK pathway. Plays a critical role in orchestrating the pro-B cell to pre-B cell transition. May play an important role in BCR-induced B-cell apoptosis. {ECO:0000269|PubMed:10583958, ECO:0000269|PubMed:15270728, ECO:0000269|PubMed:16912232, ECO:0000269|PubMed:9697839}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000224337, ENST00000371176, 
ENST00000413476, ENST00000427367, 
ENST00000495266, 
ENST00000590564, 
ENST00000355537, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 6=25221 X 13 X 13=3549
# samples 725
** MAII scorelog2(7/252*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(25/3549*10)=-3.82741257439886
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BLNK [Title/Abstract] AND ZNF536 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BLNK [Title/Abstract] AND ZNF536 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BLNK(98002491)-ZNF536(31025754), # samples:3
Anticipated loss of major functional domain due to fusion event.BLNK-ZNF536 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.
BLNK-ZNF536 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.
BLNK-ZNF536 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.
BLNK-ZNF536 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
HgeneBLNK

GO:0035556

intracellular signal transduction

9341187

TgeneZNF536

GO:0000122

negative regulation of transcription by RNA polymerase II

19398580



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/chr10:98002491/chr19:31025754)
- 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 BLNK (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 ZNF536 (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)
ENST00000224337BLNKchr1098002491-ENST00000355537ZNF536chr1931025754+29333051032037644
ENST00000371176BLNKchr1098002491-ENST00000355537ZNF536chr1931025754+29333051032037644
ENST00000427367BLNKchr1098002491-ENST00000355537ZNF536chr1931025754+29693411392073644
ENST00000413476BLNKchr1098002491-ENST00000355537ZNF536chr1931025754+29693411392073644
ENST00000495266BLNKchr1098002491-ENST00000355537ZNF536chr1931025754+279116301895631

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
ENST00000224337ENST00000355537BLNKchr1098002491-ZNF536chr1931025754+0.0005179950.999482
ENST00000371176ENST00000355537BLNKchr1098002491-ZNF536chr1931025754+0.0005179950.999482
ENST00000427367ENST00000355537BLNKchr1098002491-ZNF536chr1931025754+0.0005298250.9994702
ENST00000413476ENST00000355537BLNKchr1098002491-ZNF536chr1931025754+0.0005298250.9994702
ENST00000495266ENST00000355537BLNKchr1098002491-ZNF536chr1931025754+0.000491880.99950814

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 BLNK-ZNF536

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BLNKchr1098002491ZNF536chr193102575416352KVKAPPSVPRRDYASDIGEEAGRSAG
BLNKchr1098002491ZNF536chr193102575430565KVKAPPSVPRRDYASDIGEEAGRSAG
BLNKchr1098002491ZNF536chr193102575434165KVKAPPSVPRRDYASDIGEEAGRSAG

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Potential FusionNeoAntigen Information of BLNK-ZNF536 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.
BLNK-ZNF536_98002491_31025754.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)
BLNK-ZNF536chr1098002491chr1931025754305HLA-C08:04YASDIGEEA0.98880.97591221
BLNK-ZNF536chr1098002491chr1931025754305HLA-C08:13YASDIGEEA0.98880.97591221
BLNK-ZNF536chr1098002491chr1931025754305HLA-C08:03YASDIGEEA0.8150.97911221
BLNK-ZNF536chr1098002491chr1931025754305HLA-C03:06YASDIGEEA0.98790.99441221
BLNK-ZNF536chr1098002491chr1931025754305HLA-C08:01YASDIGEEA0.8150.97911221
BLNK-ZNF536chr1098002491chr1931025754305HLA-B78:02YASDIGEEA0.32330.87211221

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Potential FusionNeoAntigen Information of BLNK-ZNF536 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.
BLNK-ZNF536_98002491_31025754.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)
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0401RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0401PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0433RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0433PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0434RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0434PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0435RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0435PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0438RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0438PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0462RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0462PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0463RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0463PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0464RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0464PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0466RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0466PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0472RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0472PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0472RDYASDIGEEAGRSA1025
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0472VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0474RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0476RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB1-0476PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0101RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0101PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0101VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0104RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0104PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0104VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0105RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0105PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0105VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0108RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0108PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0108VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0109RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0109PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0109VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0111RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0111PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0111VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0112RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0112PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0112VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0113RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0113PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0113VPRRDYASDIGEEAG722
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0114RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0114PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0202RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0205RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0209RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0209PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0210RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0212RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0212PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0213RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0213PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0215RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0215PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0216RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0216PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0217RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0217PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0218RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0219RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0219PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0220RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0221RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0221PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0222RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0222PRRDYASDIGEEAGR823
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0223RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0225RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0303RRDYASDIGEEAGRS924
BLNK-ZNF536chr1098002491chr1931025754305DRB3-0303PRRDYASDIGEEAGR823

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Fusion breakpoint peptide structures of BLNK-ZNF536

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
9163SVPRRDYASDIGEEBLNKZNF536chr1098002491chr1931025754305

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BLNK-ZNF536

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-B14:023BVN9163SVPRRDYASDIGEE-7.15543-7.26883
HLA-B14:023BVN9163SVPRRDYASDIGEE-4.77435-5.80965
HLA-B52:013W399163SVPRRDYASDIGEE-6.80875-6.92215
HLA-B52:013W399163SVPRRDYASDIGEE-4.20386-5.23916
HLA-A11:014UQ29163SVPRRDYASDIGEE-7.5194-8.5547
HLA-A11:014UQ29163SVPRRDYASDIGEE-6.9601-7.0735
HLA-A24:025HGA9163SVPRRDYASDIGEE-7.52403-7.63743
HLA-A24:025HGA9163SVPRRDYASDIGEE-5.82433-6.85963
HLA-B27:056PYJ9163SVPRRDYASDIGEE-3.28285-4.31815
HLA-B44:053DX89163SVPRRDYASDIGEE-5.91172-6.94702
HLA-B44:053DX89163SVPRRDYASDIGEE-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of BLNK-ZNF536

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
BLNK-ZNF536chr1098002491chr19310257541221YASDIGEEACAGACATTGGCGAGGAGGCTGGGAGAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
BLNK-ZNF536chr1098002491chr19310257541025RDYASDIGEEAGRSAACGCTTCAGACATTGGCGAGGAGGCTGGGAGATCTGCCGGCGTCC
BLNK-ZNF536chr1098002491chr1931025754722VPRRDYASDIGEEAGGAAGGGACTACGCTTCAGACATTGGCGAGGAGGCTGGGAGATCTG
BLNK-ZNF536chr1098002491chr1931025754823PRRDYASDIGEEAGRGGGACTACGCTTCAGACATTGGCGAGGAGGCTGGGAGATCTGCCG
BLNK-ZNF536chr1098002491chr1931025754924RRDYASDIGEEAGRSACTACGCTTCAGACATTGGCGAGGAGGCTGGGAGATCTGCCGGCG

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Information of the samples that have these potential fusion neoantigens of BLNK-ZNF536

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
BRCABLNK-ZNF536chr1098002491ENST00000224337chr1931025754ENST00000355537TCGA-A8-A08I-01A

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Potential target of CAR-T therapy development for BLNK-ZNF536

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 BLNK-ZNF536

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 BLNK-ZNF536

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