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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:CDC73-KCNT2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CDC73-KCNT2
FusionPDB ID: 14943
FusionGDB2.0 ID: 14943
HgeneTgene
Gene symbol

CDC73

KCNT2

Gene ID

79577

343450

Gene namecell division cycle 73potassium sodium-activated channel subfamily T member 2
SynonymsC1orf28|FIHP|HPTJT|HRPT1|HRPT2|HYXEIEE57|KCa4.2|SLICK|SLO2.1
Cytomap

1q31.2

1q31.3

Type of geneprotein-codingprotein-coding
DescriptionparafibrominFamilial isolated hyperparathyroidismPaf1/RNA polymerase II complex componentcell division cycle 73 Paf1/RNA polymerase II complex component-like proteincell division cycle 73, Paf1/RNA polymerase II complex component, homologcell divisiopotassium channel subfamily T member 2potassium channel, subfamily T, member 2sequence like an intermediate conductance potassium channel subunitsodium and chloride-activated ATP-sensitive potassium channel Slo2.1sodium-and chloride-activated ATP-sens
Modification date2020031320200322
UniProtAcc

Q6P1J9

Main function of 5'-partner protein: FUNCTION: Tumor suppressor probably involved in transcriptional and post-transcriptional control pathways. May be involved in cell cycle progression through the regulation of cyclin D1/PRAD1 expression. Component of the PAF1 complex (PAF1C) which has multiple functions during transcription by RNA polymerase II and is implicated in regulation of development and maintenance of embryonic stem cell pluripotency. PAF1C associates with RNA polymerase II through interaction with POLR2A CTD non-phosphorylated and 'Ser-2'- and 'Ser-5'-phosphorylated forms and is involved in transcriptional elongation, acting both independently and synergistically with TCEA1 and in cooperation with the DSIF complex and HTATSF1. PAF1C is required for transcription of Hox and Wnt target genes. PAF1C is involved in hematopoiesis and stimulates transcriptional activity of KMT2A/MLL1; it promotes leukemogenesis through association with KMT2A/MLL1-rearranged oncoproteins, such as KMT2A/MLL1-MLLT3/AF9 and KMT2A/MLL1-MLLT1/ENL. PAF1C is involved in histone modifications such as ubiquitination of histone H2B and methylation on histone H3 'Lys-4' (H3K4me3). PAF1C recruits the RNF20/40 E3 ubiquitin-protein ligase complex and the E2 enzyme UBE2A or UBE2B to chromatin which mediate monoubiquitination of 'Lys-120' of histone H2B (H2BK120ub1); UB2A/B-mediated H2B ubiquitination is proposed to be coupled to transcription. PAF1C is involved in mRNA 3' end formation probably through association with cleavage and poly(A) factors. In case of infection by influenza A strain H3N2, PAF1C associates with viral NS1 protein, thereby regulating gene transcription. Connects PAF1C with the cleavage and polyadenylation specificity factor (CPSF) complex and the cleavage stimulation factor (CSTF) complex, and with Wnt signaling. Involved in polyadenylation of mRNA precursors. {ECO:0000269|PubMed:15580289, ECO:0000269|PubMed:15632063, ECO:0000269|PubMed:15923622, ECO:0000269|PubMed:16630820, ECO:0000269|PubMed:16989776, ECO:0000269|PubMed:19136632, ECO:0000269|PubMed:19952111, ECO:0000269|PubMed:20178742, ECO:0000269|PubMed:20541477, ECO:0000269|PubMed:21329879}.

Q6UVM3

Main function of 5'-partner protein: FUNCTION: Outward rectifying potassium channel. Produces rapidly activating outward rectifier K(+) currents. Activated by high intracellular sodium and chloride levels (PubMed:14684870, PubMed:16687497, PubMed:29069600). Channel activity is inhibited by ATP and by inhalation anesthetics, such as isoflurane (PubMed:16687497) (By similarity). Inhibited upon stimulation of G-protein coupled receptors, such as CHRM1 and GRM1 (PubMed:16687497). {ECO:0000250|UniProtKB:Q6UVM4, ECO:0000269|PubMed:14684870, ECO:0000269|PubMed:16687497, ECO:0000269|PubMed:29069600}.
Ensembl transtripts involved in fusion geneENST idsENST00000367435, ENST00000477868, 
ENST00000294725, ENST00000451324, 
ENST00000367431, ENST00000498426, 
ENST00000609185, ENST00000367433, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 6 X 6=2887 X 6 X 5=210
# samples 87
** MAII scorelog2(8/288*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CDC73 [Title/Abstract] AND KCNT2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CDC73 [Title/Abstract] AND KCNT2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CDC73(193121574)-KCNT2(196448368), # samples:1
Anticipated loss of major functional domain due to fusion event.CDC73-KCNT2 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.
CDC73-KCNT2 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.
CDC73-KCNT2 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.
CDC73-KCNT2 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
HgeneCDC73

GO:0008285

negative regulation of cell proliferation

16989776

HgeneCDC73

GO:0010390

histone monoubiquitination

16307923

HgeneCDC73

GO:0030177

positive regulation of Wnt signaling pathway

16630820

HgeneCDC73

GO:0032968

positive regulation of transcription elongation from RNA polymerase II promoter

20178742

HgeneCDC73

GO:0033523

histone H2B ubiquitination

16307923

HgeneCDC73

GO:0045638

negative regulation of myeloid cell differentiation

20541477

HgeneCDC73

GO:0045944

positive regulation of transcription by RNA polymerase II

20178742

HgeneCDC73

GO:2000134

negative regulation of G1/S transition of mitotic cell cycle

16989776



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/chr1:193121574/chr1:196448368)
- 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 CDC73 (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 KCNT2 (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)
ENST00000367435CDC73chr1193121574+ENST00000367433KCNT2chr1196448368-66131156741671386

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
ENST00000367435ENST00000367433CDC73chr1193121574+KCNT2chr1196448368-0.0001763240.99982375

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 CDC73-KCNT2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CDC73chr1193121574KCNT2chr11964483681156383MGTYHGMTLKSVTVSVALISLFETIL

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Potential FusionNeoAntigen Information of CDC73-KCNT2 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.
CDC73-KCNT2_193121574_196448368.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)
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:13TLKSVTVSV0.99510.7197716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:17KSVTVSVAL0.99470.9456918
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:16KSVTVSVAL0.99440.7758918
CDC73-KCNT2chr1193121574chr11964483681156HLA-B57:03KSVTVSVAL0.98960.9909918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:38TLKSVTVSV0.98710.7085716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:27TLKSVTVSV0.98710.5794716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:13GMTLKSVTV0.98650.5328514
CDC73-KCNT2chr1193121574chr11964483681156HLA-A30:08TLKSVTVSV0.97490.6745716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:38GMTLKSVTV0.96590.5603514
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:11TLKSVTVSV0.94980.5519716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:30TLKSVTVSV0.94920.521716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:24TLKSVTVSV0.94920.521716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:67TLKSVTVSV0.94920.521716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:21TLKSVTVSV0.94680.6707716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:16TLKSVTVSV0.93990.6194716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:29TLKSVTVSV0.93690.5224716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:04TLKSVTVSV0.93610.5202716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:35TLKSVTVSV0.92510.5508716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:20TLKSVTVSV0.92020.5305716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B13:02TLKSVTVSV0.18290.7586716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B13:02GMTLKSVTV0.110.7562514
CDC73-KCNT2chr1193121574chr11964483681156HLA-B57:03VTVSVALISLF0.99840.97651122
CDC73-KCNT2chr1193121574chr11964483681156HLA-C15:04KSVTVSVAL0.99980.9292918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:19KSVTVSVAL0.99960.99918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C15:06KSVTVSVAL0.99960.9515918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:07KSVTVSVAL0.99960.9822918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:08KSVTVSVAL0.99930.9484918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C08:13KSVTVSVAL0.990.9725918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C08:04KSVTVSVAL0.990.9725918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C08:03KSVTVSVAL0.95140.9918918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:01TLKSVTVSV0.94920.521716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:07TLKSVTVSV0.94920.5762716
CDC73-KCNT2chr1193121574chr11964483681156HLA-C02:06KSVTVSVAL0.91130.9448918
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:04TLKSVTVSV0.86120.9707716
CDC73-KCNT2chr1193121574chr11964483681156HLA-C15:09KSVTVSVAL0.99980.9292918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C15:02KSVTVSVAL0.99960.8997918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C15:05KSVTVSVAL0.99950.9105918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:17KSVTVSVAL0.99930.9817918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:05KSVTVSVAL0.99920.9599918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:03TLKSVTVSV0.99910.6551716
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:04KSVTVSVAL0.9990.9939918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:03KSVTVSVAL0.9990.9939918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C16:02KSVTVSVAL0.9940.9957918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C16:01KSVTVSVAL0.99330.984918
CDC73-KCNT2chr1193121574chr11964483681156HLA-C03:06KSVTVSVAL0.98160.994918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A32:01KSVTVSVAL0.98080.945918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A69:01TVSVALISL0.96960.59251221
CDC73-KCNT2chr1193121574chr11964483681156HLA-C08:01KSVTVSVAL0.95140.9918918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:14TLKSVTVSV0.94880.5807716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A02:06TLKSVTVSV0.94680.6707716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:30KSVTVSVAL0.94380.823918
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:73TLKSVTVSV0.92380.8499716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B15:30TLKSVTVSV0.89660.8456716
CDC73-KCNT2chr1193121574chr11964483681156HLA-A68:02TLKSVTVSV0.8450.5123716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B08:12TLKSVTVSV0.76730.5723716
CDC73-KCNT2chr1193121574chr11964483681156HLA-B35:13KSVTVSVAL0.75260.9394918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A69:01TLKSVTVSV0.70910.7062716
CDC73-KCNT2chr1193121574chr11964483681156HLA-C17:01KSVTVSVAL0.6850.9637918
CDC73-KCNT2chr1193121574chr11964483681156HLA-B07:13KSVTVSVAL0.50980.8199918
CDC73-KCNT2chr1193121574chr11964483681156HLA-A68:02MTLKSVTVSV0.9890.6468616
CDC73-KCNT2chr1193121574chr11964483681156HLA-A69:01MTLKSVTVSV0.98430.7081616

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Potential FusionNeoAntigen Information of CDC73-KCNT2 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 CDC73-KCNT2

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
6035MTLKSVTVSVALISCDC73KCNT2chr1193121574chr11964483681156

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CDC73-KCNT2

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-B14:023BVN6035MTLKSVTVSVALIS-7.9962-8.1096
HLA-B14:023BVN6035MTLKSVTVSVALIS-5.70842-6.74372
HLA-B52:013W396035MTLKSVTVSVALIS-6.83737-6.95077
HLA-B52:013W396035MTLKSVTVSVALIS-4.4836-5.5189
HLA-A11:014UQ26035MTLKSVTVSVALIS-10.0067-10.1201
HLA-A11:014UQ26035MTLKSVTVSVALIS-9.03915-10.0745
HLA-A24:025HGA6035MTLKSVTVSVALIS-6.56204-6.67544
HLA-A24:025HGA6035MTLKSVTVSVALIS-5.42271-6.45801
HLA-B44:053DX86035MTLKSVTVSVALIS-7.85648-8.89178
HLA-B44:053DX86035MTLKSVTVSVALIS-5.3978-5.5112
HLA-A02:016TDR6035MTLKSVTVSVALIS-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CDC73-KCNT2

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
CDC73-KCNT2chr1193121574chr11964483681122VTVSVALISLFGTAACGGTTTCAGTGGCATTGATAAGTCTGTTT
CDC73-KCNT2chr1193121574chr11964483681221TVSVALISLACGGTTTCAGTGGCATTGATAAGTCTG
CDC73-KCNT2chr1193121574chr1196448368514GMTLKSVTVGGTATGACACTGAAATCTGTAACGGTT
CDC73-KCNT2chr1193121574chr1196448368616MTLKSVTVSVATGACACTGAAATCTGTAACGGTTTCAGTG
CDC73-KCNT2chr1193121574chr1196448368716TLKSVTVSVACACTGAAATCTGTAACGGTTTCAGTG
CDC73-KCNT2chr1193121574chr1196448368918KSVTVSVALAAATCTGTAACGGTTTCAGTGGCATTG

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 CDC73-KCNT2

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
SKCMCDC73-KCNT2chr1193121574ENST00000367435chr1196448368ENST00000367433TCGA-FS-A1ZU-06A

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Potential target of CAR-T therapy development for CDC73-KCNT2

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
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328229_24901136.0IntramembranePore-forming
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327229_24901112.0IntramembranePore-forming
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328138_15801136.0TransmembraneHelical%3B Name%3DSegment S3
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328165_18501136.0TransmembraneHelical%3B Name%3DSegment S4
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328199_21901136.0TransmembraneHelical%3B Name%3DSegment S5
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328257_27701136.0TransmembraneHelical%3B Name%3DSegment S6
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327138_15801112.0TransmembraneHelical%3B Name%3DSegment S3
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327165_18501112.0TransmembraneHelical%3B Name%3DSegment S4
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327199_21901112.0TransmembraneHelical%3B Name%3DSegment S5
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327257_27701112.0TransmembraneHelical%3B Name%3DSegment S6

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 CDC73-KCNT2

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 CDC73-KCNT2

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