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Fusion Protein:CDC73-KCNT2 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: CDC73-KCNT2 | FusionPDB ID: 14943 | FusionGDB2.0 ID: 14943 | Hgene | Tgene | Gene symbol | CDC73 | KCNT2 | Gene ID | 79577 | 343450 |
Gene name | cell division cycle 73 | potassium sodium-activated channel subfamily T member 2 | |
Synonyms | C1orf28|FIHP|HPTJT|HRPT1|HRPT2|HYX | EIEE57|KCa4.2|SLICK|SLO2.1 | |
Cytomap | 1q31.2 | 1q31.3 | |
Type of gene | protein-coding | protein-coding | |
Description | parafibrominFamilial 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 divisio | potassium 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 date | 20200313 | 20200322 | |
UniProtAcc | Q6P1J9 | Q6UVM3 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000367435, ENST00000477868, | ENST00000294725, ENST00000451324, ENST00000367431, ENST00000498426, ENST00000609185, ENST00000367433, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 8 X 6 X 6=288 | 7 X 6 X 5=210 |
# samples | 8 | 7 | |
** MAII score | log2(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 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: CDC73 [Title/Abstract] AND KCNT2 [Title/Abstract] AND fusion [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | CDC73 | GO:0008285 | negative regulation of cell proliferation | 16989776 |
Hgene | CDC73 | GO:0010390 | histone monoubiquitination | 16307923 |
Hgene | CDC73 | GO:0030177 | positive regulation of Wnt signaling pathway | 16630820 |
Hgene | CDC73 | GO:0032968 | positive regulation of transcription elongation from RNA polymerase II promoter | 20178742 |
Hgene | CDC73 | GO:0033523 | histone H2B ubiquitination | 16307923 |
Hgene | CDC73 | GO:0045638 | negative regulation of myeloid cell differentiation | 20541477 |
Hgene | CDC73 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 20178742 |
Hgene | CDC73 | GO:2000134 | negative regulation of G1/S transition of mitotic cell cycle | 16989776 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | SKCM | TCGA-FS-A1ZU-06A | CDC73 | chr1 | 193121574 | + | KCNT2 | chr1 | 196448368 | - |
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Fusion ORF Analysis |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000367435 | CDC73 | chr1 | 193121574 | + | ENST00000367433 | KCNT2 | chr1 | 196448368 | - | 6613 | 1156 | 7 | 4167 | 1386 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000367435 | ENST00000367433 | CDC73 | chr1 | 193121574 | + | KCNT2 | chr1 | 196448368 | - | 0.000176324 | 0.99982375 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >14943_14943_1_CDC73-KCNT2_CDC73_chr1_193121574_ENST00000367435_KCNT2_chr1_196448368_ENST00000367433_length(amino acids)=1386AA_BP=383 MGGYCPCCCRRRGRLLVLLLLVRRGGEGGGGRGRGDKRRRRQARRQRRRPEPAEARGGKMADVLSVLRQYNIQKKEIVVKGDEVIFGEFS WPKNVKTNYVVWGTGKEGQPREYYTLDSILFLLNNVHLSHPVYVRRAATENIPVVRRPDRKDLLGYLNGEASTSASIDRSAPLEIGLQRS TQVKRAADEVLAEAKKPRIEDEECVRLDKERLAARLEGHKEGIVQTEQIRSLSEAMSVEKIAAIKAKIMAKKRSTIKTDLDDDITALKQR SFVDAEVDVTRDIVSRERVWRTRTTILQSTGKNFSKNIFAILQSVKAREEGRAPEQRPAPNAAPVDPTLRTKQPIPAAYNRYDQERFKGK EETEGFKIDTMGTYHGMTLKSVTVSVALISLFETILLGYLSYKGNIWEQILRIPFILEIINAVPFIISIFWPSLRNLFVPVFLNCWLAKH ALENMINDLHRAIQRTQSAMFNQVLILISTLLCLIFTCICGIQHLERIGKKLNLFDSLYFCIVTFSTVGFGDVTPETWSSKLFVVAMICV ALVVLPIQFEQLAYLWMERQKSGGNYSRHRAQTEKHVVLCVSSLKIDLLMDFLNEFYAHPRLQDYYVVILCPTEMDVQVRRVLQIPMWSQ RVIYLQGSALKDQDLLRAKMDDAEACFILSSRCEVDRTSSDHQTILRAWAVKDFAPNCPLYVQILKPENKFHIKFADHVVCEEEFKYAML ALNCICPATSTLITLLVHTSRGQEGQQSPEQWQKMYGRCSGNEVYHIVLEESTFFAEYEGKSFTYASFHAHKKFGVCLIGVRREDNKNIL LNPGPRYIMNSTDICFYINITKEENSAFKNQDQQRKSNVSRSFYHGPSRLPVHSIIASMGTVAIDLQDTSCRSASGPTLSLPTEGSKEIR RPSIAPVLEVADTSSIQTCDLLSDQSEDETTPDEEMSSNLEYAKGYPPYSPYIGSSPTFCHLLHEKVPFCCLRLDKSCQHNYYEDAKAYG FKNKLIIVAAETAGNGLYNFIVPLRAYYRPKKELNPIVLLLDNPLDDLLRCGVTFAANMVVVDKESTMSAEEDYMADAKTIVNVQTLFRL FSSLSIITELTHPANMRFMQFRAKDCYSLALSKLEKKERERGSNLAFMFRLPFAAGRVFSISMLDTLLYQSFVKDYMISITRLLLGLDTT PGSGFLCSMKITADDLWIRTYARLYQKLCSSTGDVPIGIYRTESQKLTTSESQISISVEEWEDTKDSKEQGHHRSNHRNSTSSDQSDHPL LRRKSMQWARRLSRKGPKHSGKTAEKITQQRLNLYRRSERQELAELVKNRMKHLGLSTVGYDEMNDHQSTLSYILINPSPDTRIELNDVV -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() 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. |
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Hgene | Tgene |
CDC73 | KCNT2 |
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}. | 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}. |
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- Retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | CDC73 | chr1:193121574 | chr1:196448368 | ENST00000367435 | + | 10 | 17 | 125_139 | 324.0 | 532.0 | Motif | Note=Nuclear localization signal |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 422_543 | 108.0 | 1136.0 | Domain | Note=RCK N-terminal | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 422_543 | 108.0 | 1112.0 | Domain | Note=RCK N-terminal | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 229_249 | 108.0 | 1136.0 | Intramembrane | Pore-forming | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 229_249 | 108.0 | 1112.0 | Intramembrane | Pore-forming | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 1025_1032 | 108.0 | 1136.0 | Nucleotide binding | ATP | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 1025_1032 | 108.0 | 1112.0 | Nucleotide binding | ATP | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 123_137 | 108.0 | 1136.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 159_164 | 108.0 | 1136.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 186_198 | 108.0 | 1136.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 220_228 | 108.0 | 1136.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 250_256 | 108.0 | 1136.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 278_1135 | 108.0 | 1136.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 123_137 | 108.0 | 1112.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 159_164 | 108.0 | 1112.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 186_198 | 108.0 | 1112.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 220_228 | 108.0 | 1112.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 250_256 | 108.0 | 1112.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 278_1135 | 108.0 | 1112.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 138_158 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S3 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 165_185 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S4 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 199_219 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S5 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 257_277 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S6 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 138_158 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S3 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 165_185 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S4 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 199_219 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S5 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 257_277 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S6 |
- Not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | CDC73 | chr1:193121574 | chr1:196448368 | ENST00000367435 | + | 10 | 17 | 361_364 | 324.0 | 532.0 | Compositional bias | Note=Poly-Ile |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 1_63 | 108.0 | 1136.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 85_101 | 108.0 | 1136.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 1_63 | 108.0 | 1112.0 | Topological domain | Cytoplasmic | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 85_101 | 108.0 | 1112.0 | Topological domain | Extracellular | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 102_122 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S2 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000294725 | 3 | 28 | 64_84 | 108.0 | 1136.0 | Transmembrane | Helical%3B Name%3DSegment S1 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 102_122 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S2 | |
Tgene | KCNT2 | chr1:193121574 | chr1:196448368 | ENST00000367433 | 3 | 27 | 64_84 | 108.0 | 1112.0 | Transmembrane | Helical%3B Name%3DSegment S1 |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
CDC73 | |
KCNT2 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Hgene | CDC73 | chr1:193121574 | chr1:196448368 | ENST00000367435 | + | 10 | 17 | 200_531 | 324.0 | 532.0 | POLR2A and PAF1 |
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Related Drugs to CDC73-KCNT2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to CDC73-KCNT2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |