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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:CDC73-KCNT2

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

Q6UVM3

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
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)

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 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 Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4SKCMTCGA-FS-A1ZU-06ACDC73chr1

193121574

+KCNT2chr1

196448368

-


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Fusion ORF Analysis


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

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>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


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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CDC73

Q6P1J9

KCNT2

Q6UVM3

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}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCDC73chr1:193121574chr1:196448368ENST00000367435+1017125_139324.0532.0MotifNote=Nuclear localization signal
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328422_543108.01136.0DomainNote=RCK N-terminal
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327422_543108.01112.0DomainNote=RCK N-terminal
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328229_249108.01136.0IntramembranePore-forming
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327229_249108.01112.0IntramembranePore-forming
TgeneKCNT2chr1:193121574chr1:196448368ENST000002947253281025_1032108.01136.0Nucleotide bindingATP
TgeneKCNT2chr1:193121574chr1:196448368ENST000003674333271025_1032108.01112.0Nucleotide bindingATP
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328123_137108.01136.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328159_164108.01136.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328186_198108.01136.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328220_228108.01136.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328250_256108.01136.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328278_1135108.01136.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327123_137108.01112.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327159_164108.01112.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327186_198108.01112.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327220_228108.01112.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327250_256108.01112.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327278_1135108.01112.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328138_158108.01136.0TransmembraneHelical%3B Name%3DSegment S3
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328165_185108.01136.0TransmembraneHelical%3B Name%3DSegment S4
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328199_219108.01136.0TransmembraneHelical%3B Name%3DSegment S5
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328257_277108.01136.0TransmembraneHelical%3B Name%3DSegment S6
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327138_158108.01112.0TransmembraneHelical%3B Name%3DSegment S3
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327165_185108.01112.0TransmembraneHelical%3B Name%3DSegment S4
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327199_219108.01112.0TransmembraneHelical%3B Name%3DSegment S5
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327257_277108.01112.0TransmembraneHelical%3B Name%3DSegment S6

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCDC73chr1:193121574chr1:196448368ENST00000367435+1017361_364324.0532.0Compositional biasNote=Poly-Ile
TgeneKCNT2chr1:193121574chr1:196448368ENST000002947253281_63108.01136.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST0000029472532885_101108.01136.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST000003674333271_63108.01112.0Topological domainCytoplasmic
TgeneKCNT2chr1:193121574chr1:196448368ENST0000036743332785_101108.01112.0Topological domainExtracellular
TgeneKCNT2chr1:193121574chr1:196448368ENST00000294725328102_122108.01136.0TransmembraneHelical%3B Name%3DSegment S2
TgeneKCNT2chr1:193121574chr1:196448368ENST0000029472532864_84108.01136.0TransmembraneHelical%3B Name%3DSegment S1
TgeneKCNT2chr1:193121574chr1:196448368ENST00000367433327102_122108.01112.0TransmembraneHelical%3B Name%3DSegment S2
TgeneKCNT2chr1:193121574chr1:196448368ENST0000036743332764_84108.01112.0TransmembraneHelical%3B Name%3DSegment S1


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CDC73
KCNT2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneCDC73chr1:193121574chr1:196448368ENST00000367435+1017200_531324.0532.0POLR2A and PAF1


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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