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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:DIS3-KLF12

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DIS3-KLF12
FusionPDB ID: 22898
FusionGDB2.0 ID: 22898
HgeneTgene
Gene symbol

DIS3

KLF12

Gene ID

22894

11278

Gene nameDIS3 homolog, exosome endoribonuclease and 3'-5' exoribonucleaseKruppel like factor 12
Synonyms2810028N01Rik|EXOSC11|KIAA1008|RRP44|dis3pAP-2rep|AP2REP|HSPC122
Cytomap

13q21.33

13q22.1

Type of geneprotein-codingprotein-coding
Descriptionexosome complex exonuclease RRP44DIS3 exosome endoribonuclease and 3'-5' exoribonucleaseDIS3 mitotic control homologexosome component 11mitotic control protein dis3 homologribosomal RNA-processing protein 44Krueppel-like factor 12AP-2 repressorAP-2rep transcription factorKLF12 zinc finger transcriptional repressortranscriptional repressor AP-2rep
Modification date2020031320200313
UniProtAcc

Q8IYB7

Main function of 5'-partner protein: FUNCTION: 3'-5'-exoribonuclease that specifically recognizes RNAs polyuridylated at their 3' end and mediates their degradation. Component of an exosome-independent RNA degradation pathway that mediates degradation of both mRNAs and miRNAs that have been polyuridylated by a terminal uridylyltransferase, such as ZCCHC11/TUT4. Mediates degradation of cytoplasmic mRNAs that have been deadenylated and subsequently uridylated at their 3'. Mediates degradation of uridylated pre-let-7 miRNAs, contributing to the maintenance of embryonic stem (ES) cells. Essential for correct mitosis, and negatively regulates cell proliferation. {ECO:0000255|HAMAP-Rule:MF_03045, ECO:0000269|PubMed:23756462, ECO:0000269|PubMed:24141620}.

Q9Y4X4

Main function of 5'-partner protein: FUNCTION: Confers strong transcriptional repression to the AP-2-alpha gene. Binds to a regulatory element (A32) in the AP-2-alpha gene promoter.
Ensembl transtripts involved in fusion geneENST idsENST00000377767, ENST00000377780, 
ENST00000545453, ENST00000475871, 
ENST00000472022, ENST00000377666, 
ENST00000377669, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score2 X 3 X 2=1213 X 13 X 6=1014
# samples 316
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(16/1014*10)=-2.66391384211598
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: DIS3 [Title/Abstract] AND KLF12 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: DIS3 [Title/Abstract] AND KLF12 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DIS3(73345933)-KLF12(74420510), # samples:2
Anticipated loss of major functional domain due to fusion event.DIS3-KLF12 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.
DIS3-KLF12 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.
DIS3-KLF12 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
DIS3-KLF12 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
DIS3-KLF12 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
DIS3-KLF12 seems lost the major protein functional domain in Tgene partner, which is a transcription factor 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
TgeneKLF12

GO:0000122

negative regulation of transcription by RNA polymerase II

16615998



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/chr13:73345933/chr13:74420510)
- 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 DIS3 (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 KLF12 (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)
ENST00000377767DIS3chr1373345933-ENST00000377669KLF12chr1374420510-1219317061012791896
ENST00000377767DIS3chr1373345933-ENST00000377666KLF12chr1374420510-288317061012791896
ENST00000377780DIS3chr1373345933-ENST00000377669KLF12chr1374420510-120951608932693866
ENST00000377780DIS3chr1373345933-ENST00000377666KLF12chr1374420510-27851608932693866
ENST00000377767DIS3chr1373345932-ENST00000377669KLF12chr1374420510-1219317061012791896
ENST00000377767DIS3chr1373345932-ENST00000377666KLF12chr1374420510-288317061012791896
ENST00000377780DIS3chr1373345932-ENST00000377669KLF12chr1374420510-120951608932693866
ENST00000377780DIS3chr1373345932-ENST00000377666KLF12chr1374420510-27851608932693866

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
ENST00000377767ENST00000377669DIS3chr1373345933-KLF12chr1374420510-0.0004687040.99953127
ENST00000377767ENST00000377666DIS3chr1373345933-KLF12chr1374420510-0.0013681540.9986318
ENST00000377780ENST00000377669DIS3chr1373345933-KLF12chr1374420510-0.0004503510.99954957
ENST00000377780ENST00000377666DIS3chr1373345933-KLF12chr1374420510-0.0014334430.99856657
ENST00000377767ENST00000377669DIS3chr1373345932-KLF12chr1374420510-0.0004687040.99953127
ENST00000377767ENST00000377666DIS3chr1373345932-KLF12chr1374420510-0.0013681540.9986318
ENST00000377780ENST00000377669DIS3chr1373345932-KLF12chr1374420510-0.0004503510.99954957
ENST00000377780ENST00000377666DIS3chr1373345932-KLF12chr1374420510-0.0014334430.99856657

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 DIS3-KLF12

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
DIS3chr1373345932KLF12chr13744205101608505SARRGTTVYLCEKSPNVHNYPDMEAV
DIS3chr1373345932KLF12chr13744205101706535SARRGTTVYLCEKSPNVHNYPDMEAV
DIS3chr1373345933KLF12chr13744205101608505SARRGTTVYLCEKSPNVHNYPDMEAV
DIS3chr1373345933KLF12chr13744205101706535SARRGTTVYLCEKSPNVHNYPDMEAV

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Potential FusionNeoAntigen Information of DIS3-KLF12 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.
DIS3-KLF12_73345932_74420510.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)
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:22YLCEKSPNV0.9990.6851817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:30YLCEKSPNV0.99810.8191817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:24YLCEKSPNV0.99810.8191817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:60YLCEKSPNV0.99810.7897817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:11YLCEKSPNV0.99810.8462817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:67YLCEKSPNV0.99810.8191817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:13YLCEKSPNV0.99810.8033817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:21YLCEKSPNV0.9980.8855817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:27YLCEKSPNV0.9980.7553817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:16YLCEKSPNV0.99660.6554817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:04YLCEKSPNV0.99480.8259817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:17YLCEKSPNV0.99140.5239817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:38YLCEKSPNV0.99060.7215817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:29YLCEKSPNV0.98820.82817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:35YLCEKSPNV0.98520.8426817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:20YLCEKSPNV0.9830.8248817
DIS3-KLF12chr1373345932chr13744205101706HLA-B08:09YLCEKSPNV0.89470.6748817
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:03EKSPNVHNY0.24450.58731120
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:18EKSPNVHNY0.23660.581120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:01EKSPNVHNY0.13040.91151120
DIS3-KLF12chr1373345932chr13744205101706HLA-B13:02YLCEKSPNV0.03330.7084817
DIS3-KLF12chr1373345932chr13744205101706HLA-B44:03CEKSPNVHNY0.99780.87171020
DIS3-KLF12chr1373345932chr13744205101706HLA-C15:04KSPNVHNY0.9960.8281220
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:05YLCEKSPNV0.99880.5299817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:07YLCEKSPNV0.99810.8129817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:01YLCEKSPNV0.99810.8191817
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:95EKSPNVHNY0.8580.54161120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:27EKSPNVHNY0.73210.89431120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:19EKSPNVHNY0.68460.54021120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:80EKSPNVHNY0.62980.81381120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:67EKSPNVHNY0.62980.81381120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:10EKSPNVHNY0.59840.82831120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:46EKSPNVHNY0.52560.68791120
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:21EKSPNVHNY0.4170.841120
DIS3-KLF12chr1373345932chr13744205101706HLA-C12:16EKSPNVHNY0.01480.90761120
DIS3-KLF12chr1373345932chr13744205101706HLA-C15:09KSPNVHNY0.9960.8281220
DIS3-KLF12chr1373345932chr13744205101706HLA-C16:02KSPNVHNY0.95680.98391220
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:03YLCEKSPNV0.99920.8052817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:14YLCEKSPNV0.9980.8238817
DIS3-KLF12chr1373345932chr13744205101706HLA-A02:06YLCEKSPNV0.9980.8855817
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:01EKSPNVHNY0.85270.51691120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:22EKSPNVHNY0.63880.57751120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:02EKSPNVHNY0.62980.81381120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:17EKSPNVHNY0.59810.941120
DIS3-KLF12chr1373345932chr13744205101706HLA-B35:20EKSPNVHNY0.5720.81911120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:11EKSPNVHNY0.44290.83711120
DIS3-KLF12chr1373345932chr13744205101706HLA-B48:02EKSPNVHNY0.42410.7851120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:04EKSPNVHNY0.38510.91891120
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:12EKSPNVHNY0.2650.87271120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:03EKSPNVHNY0.26420.90421120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:07EKSPNVHNY0.17380.8811120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:08EKSPNVHNY0.16690.77261120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:06EKSPNVHNY0.14920.89461120
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:05EKSPNVHNY0.13040.91151120
DIS3-KLF12chr1373345932chr13744205101706HLA-C07:04YLCEKSPNV0.11760.9734817
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:53EKSPNVHNY0.03290.80461120
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:54EKSPNVHNY0.0220.78451120
DIS3-KLF12chr1373345932chr13744205101706HLA-C06:17EKSPNVHNY0.00140.98571120
DIS3-KLF12chr1373345932chr13744205101706HLA-C06:02EKSPNVHNY0.00140.98571120
DIS3-KLF12chr1373345932chr13744205101706HLA-B44:26CEKSPNVHNY0.99780.87171020
DIS3-KLF12chr1373345932chr13744205101706HLA-B44:07CEKSPNVHNY0.99780.87171020
DIS3-KLF12chr1373345932chr13744205101706HLA-B44:13CEKSPNVHNY0.99780.87171020
DIS3-KLF12chr1373345932chr13744205101706HLA-B15:53CEKSPNVHNY0.98710.73461020
DIS3-KLF12chr1373345932chr13744205101706HLA-B18:11CEKSPNVHNY0.74740.8311020

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Potential FusionNeoAntigen Information of DIS3-KLF12 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.
DIS3-KLF12_73345932_74420510.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)
DIS3-KLF12chr1373345932chr13744205101706DRB1-0111TTVYLCEKSPNVHNY520
DIS3-KLF12chr1373345932chr13744205101706DRB1-0111GTTVYLCEKSPNVHN419
DIS3-KLF12chr1373345932chr13744205101706DRB1-0113TTVYLCEKSPNVHNY520
DIS3-KLF12chr1373345932chr13744205101706DRB1-0113GTTVYLCEKSPNVHN419
DIS3-KLF12chr1373345932chr13744205101706DRB1-0473EKSPNVHNYPDMEAV1126
DIS3-KLF12chr1373345932chr13744205101706DRB1-1507EKSPNVHNYPDMEAV1126
DIS3-KLF12chr1373345932chr13744205101706DRB1-1512EKSPNVHNYPDMEAV1126
DIS3-KLF12chr1373345932chr13744205101706DRB1-1548EKSPNVHNYPDMEAV1126

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Fusion breakpoint peptide structures of DIS3-KLF12

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
9746TVYLCEKSPNVHNYDIS3KLF12chr1373345932chr13744205101706

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of DIS3-KLF12

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-B14:023BVN9746TVYLCEKSPNVHNY-7.02924-7.14264
HLA-B14:023BVN9746TVYLCEKSPNVHNY-3.38077-4.41607
HLA-B52:013W399746TVYLCEKSPNVHNY-6.41355-6.52695
HLA-B52:013W399746TVYLCEKSPNVHNY-4.44188-5.47718
HLA-A24:025HGA9746TVYLCEKSPNVHNY-7.76595-8.80125
HLA-A24:025HGA9746TVYLCEKSPNVHNY-7.30892-7.42232
HLA-B44:053DX89746TVYLCEKSPNVHNY-5.65486-5.76826
HLA-B44:053DX89746TVYLCEKSPNVHNY-2.95775-3.99305

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Vaccine Design for the FusionNeoAntigens of DIS3-KLF12

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
DIS3-KLF12chr1373345932chr13744205101020CEKSPNVHNYTGTGAAAAGTCTCCAAACGTCCACAACTAT
DIS3-KLF12chr1373345932chr13744205101120EKSPNVHNYGAAAAGTCTCCAAACGTCCACAACTAT
DIS3-KLF12chr1373345932chr13744205101220KSPNVHNYAAGTCTCCAAACGTCCACAACTAT
DIS3-KLF12chr1373345932chr1374420510817YLCEKSPNVTATCTTTGTGAAAAGTCTCCAAACGTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
DIS3-KLF12chr1373345932chr13744205101126EKSPNVHNYPDMEAVGAAAAGTCTCCAAACGTCCACAACTATCCCGATATGGAAGCCGTT
DIS3-KLF12chr1373345932chr1374420510419GTTVYLCEKSPNVHNGGAACAACTGTGTATCTTTGTGAAAAGTCTCCAAACGTCCACAAC
DIS3-KLF12chr1373345932chr1374420510520TTVYLCEKSPNVHNYACAACTGTGTATCTTTGTGAAAAGTCTCCAAACGTCCACAACTAT

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Information of the samples that have these potential fusion neoantigens of DIS3-KLF12

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
STADDIS3-KLF12chr1373345932ENST00000377767chr1374420510ENST00000377666TCGA-VQ-A922

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Potential target of CAR-T therapy development for DIS3-KLF12

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 DIS3-KLF12

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 DIS3-KLF12

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