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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:UVRAG-CMPK1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: UVRAG-CMPK1
FusionPDB ID: 97784
FusionGDB2.0 ID: 97784
HgeneTgene
Gene symbol

UVRAG

CMPK1

Gene ID

7405

51727

Gene nameUV radiation resistance associatedcytidine/uridine monophosphate kinase 1
SynonymsDHTX|VPS38|p63CK|CMK|CMPK|UMK|UMP-CMPK|UMPK
Cytomap

11q13.5

1p33

Type of geneprotein-codingprotein-coding
DescriptionUV radiation resistance-associated gene proteinbeclin 1 binding proteindisrupted in heterotaxyUMP-CMP kinaseUMP/CMP kinasecytidine monophosphate (UMP-CMP) kinase 1, cytosoliccytidylate kinasedCMP kinasedeoxycytidylate kinasenucleoside-diphosphate kinaseuridine monophosphate kinaseuridine monophosphate/cytidine monophosphate kinase
Modification date2020031320200313
UniProtAcc.

P30085

Ensembl transtripts involved in fusion geneENST idsENST00000356136, ENST00000528420, 
ENST00000533454, ENST00000525872, 
ENST00000531818, ENST00000532130, 
ENST00000538870, ENST00000539288, 
ENST00000450808, ENST00000471289, 
ENST00000371873, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score41 X 18 X 15=110708 X 7 X 4=224
# samples 499
** MAII scorelog2(49/11070*10)=-4.49772966266634
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/224*10)=-1.31550182572793
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: UVRAG [Title/Abstract] AND CMPK1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)UVRAG(75672593)-CMPK1(47834141), # samples:3
Anticipated loss of major functional domain due to fusion event.UVRAG-CMPK1 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.
UVRAG-CMPK1 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.
UVRAG-CMPK1 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.
UVRAG-CMPK1 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
HgeneUVRAG

GO:0071900

regulation of protein serine/threonine kinase activity

22542840

HgeneUVRAG

GO:0097352

autophagosome maturation

28306502

HgeneUVRAG

GO:0097680

double-strand break repair via classical nonhomologous end joining

22542840

TgeneCMPK1

GO:0006165

nucleoside diphosphate phosphorylation

23416111

TgeneCMPK1

GO:0009142

nucleoside triphosphate biosynthetic process

23416111


check buttonFusion gene breakpoints across UVRAG (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 CMPK1 (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
ChimerDB4STADTCGA-RD-A8N4-01AUVRAGchr11

75672593

-CMPK1chr1

47834141

+
ChimerDB4STADTCGA-RD-A8N4-01AUVRAGchr11

75672593

+CMPK1chr1

47834141

+
ChimerDB4STADTCGA-RD-A8N4UVRAGchr11

75672593

+CMPK1chr1

47834140

+


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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)
ENST00000356136UVRAGchr1175672593+ENST00000371873CMPK1chr147834141+35509401631455430
ENST00000528420UVRAGchr1175672593+ENST00000371873CMPK1chr147834141+3291681961196366
ENST00000356136UVRAGchr1175672593+ENST00000371873CMPK1chr147834140+35509401631455430
ENST00000528420UVRAGchr1175672593+ENST00000371873CMPK1chr147834140+3291681961196366

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
ENST00000356136ENST00000371873UVRAGchr1175672593+CMPK1chr147834141+0.0001022870.9998977
ENST00000528420ENST00000371873UVRAGchr1175672593+CMPK1chr147834141+0.0004829070.9995171
ENST00000356136ENST00000371873UVRAGchr1175672593+CMPK1chr147834140+0.0001022870.9998977
ENST00000528420ENST00000371873UVRAGchr1175672593+CMPK1chr147834140+0.0004829070.9995171

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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

>97784_97784_1_UVRAG-CMPK1_UVRAG_chr11_75672593_ENST00000356136_CMPK1_chr1_47834140_ENST00000371873_length(amino acids)=430AA_BP=259
MVGGGKGAAADAGRVPAPPLGGPWIEMSASASVGGPVPQPPPGPAAALPPGSAARALHVELPSQQRRLRHLRNIAARNIVNRNGHQLLDT
YFTLHLCSTEKIYKEFYRSEVIKNSLNPTWRSLDFGIMPDRLDTSVSCFVVKIWGGKENIYQLLIEWKVCLDGLKYLGQQIHARNQNEII
FGLNDGYYGAPFEHKGYSNAQKTILLQVDQNCVRNSYDVFSLLRLHRAQCAIKQTQVTVQKIGKEIEEKLRLTSTSNELKYGYTHLSAGE
LLRDERKNPDSQYGELIEKYIKEGKIVPVEITISLLKREMDQTMAANAQKNKFLIDGFPRNQDNLQGWNKTMDGKADVSFVLFFDCNNEI

--------------------------------------------------------------

>97784_97784_2_UVRAG-CMPK1_UVRAG_chr11_75672593_ENST00000356136_CMPK1_chr1_47834141_ENST00000371873_length(amino acids)=430AA_BP=259
MVGGGKGAAADAGRVPAPPLGGPWIEMSASASVGGPVPQPPPGPAAALPPGSAARALHVELPSQQRRLRHLRNIAARNIVNRNGHQLLDT
YFTLHLCSTEKIYKEFYRSEVIKNSLNPTWRSLDFGIMPDRLDTSVSCFVVKIWGGKENIYQLLIEWKVCLDGLKYLGQQIHARNQNEII
FGLNDGYYGAPFEHKGYSNAQKTILLQVDQNCVRNSYDVFSLLRLHRAQCAIKQTQVTVQKIGKEIEEKLRLTSTSNELKYGYTHLSAGE
LLRDERKNPDSQYGELIEKYIKEGKIVPVEITISLLKREMDQTMAANAQKNKFLIDGFPRNQDNLQGWNKTMDGKADVSFVLFFDCNNEI

--------------------------------------------------------------

>97784_97784_3_UVRAG-CMPK1_UVRAG_chr11_75672593_ENST00000528420_CMPK1_chr1_47834140_ENST00000371873_length(amino acids)=366AA_BP=195
MRRLRHLRNIAARNIVNRNGHQLLDTYFTLHLCSTEKIYKEFYRSEVIKNSLNPTWRSLDFGIMPDRLDTSVSCFVVKIWGGKENIYQLL
IEWKVCLDGLKYLGQQIHARNQNEIIFGLNDGYYGAPFEHKGYSNAQKTILLQVDQNCVRNSYDVFSLLRLHRAQCAIKQTQVTVQKIGK
EIEEKLRLTSTSNELKYGYTHLSAGELLRDERKNPDSQYGELIEKYIKEGKIVPVEITISLLKREMDQTMAANAQKNKFLIDGFPRNQDN
LQGWNKTMDGKADVSFVLFFDCNNEICIERCLERGKSSGRSDDNRESLEKRIQTYLQSTKPIIDLYEEMGKVKKIDASKSVDEVFDEVVQ

--------------------------------------------------------------

>97784_97784_4_UVRAG-CMPK1_UVRAG_chr11_75672593_ENST00000528420_CMPK1_chr1_47834141_ENST00000371873_length(amino acids)=366AA_BP=195
MRRLRHLRNIAARNIVNRNGHQLLDTYFTLHLCSTEKIYKEFYRSEVIKNSLNPTWRSLDFGIMPDRLDTSVSCFVVKIWGGKENIYQLL
IEWKVCLDGLKYLGQQIHARNQNEIIFGLNDGYYGAPFEHKGYSNAQKTILLQVDQNCVRNSYDVFSLLRLHRAQCAIKQTQVTVQKIGK
EIEEKLRLTSTSNELKYGYTHLSAGELLRDERKNPDSQYGELIEKYIKEGKIVPVEITISLLKREMDQTMAANAQKNKFLIDGFPRNQDN
LQGWNKTMDGKADVSFVLFFDCNNEICIERCLERGKSSGRSDDNRESLEKRIQTYLQSTKPIIDLYEEMGKVKKIDASKSVDEVFDEVVQ

--------------------------------------------------------------

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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/chr11:75672593/chr1:47834141)
- 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
.CMPK1

P30085

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Catalyzes the phosphorylation of pyrimidine nucleoside monophosphates at the expense of ATP. Plays an important role in de novo pyrimidine nucleotide biosynthesis. Has preference for UMP and CMP as phosphate acceptors. Also displays broad nucleoside diphosphate kinase activity. {ECO:0000255|HAMAP-Rule:MF_03172, ECO:0000269|PubMed:10462544, ECO:0000269|PubMed:11912132, ECO:0000269|PubMed:23416111}.

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
HgeneUVRAGchr11:75672593chr1:47834140ENST00000356136+71523_149233.0700.0DomainC2
HgeneUVRAGchr11:75672593chr1:47834141ENST00000356136+71523_149233.0700.0DomainC2
TgeneCMPK1chr11:75672593chr1:47834140ENST000003718730661_6357.0229.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834140ENST000003718730693_9657.0229.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834140ENST000004508080513_180180.0Nucleotide bindingATP
TgeneCMPK1chr11:75672593chr1:47834140ENST000004508080561_630180.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834140ENST000004508080593_960180.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST000003718730661_6357.0229.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST000003718730693_9657.0229.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST000004508080513_180180.0Nucleotide bindingATP
TgeneCMPK1chr11:75672593chr1:47834141ENST000004508080561_630180.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST000004508080593_960180.0Nucleotide bindingNMP
TgeneCMPK1chr11:75672593chr1:47834140ENST0000037187306133_14357.0229.0RegionLID
TgeneCMPK1chr11:75672593chr1:47834140ENST0000045080805133_1430180.0RegionLID
TgeneCMPK1chr11:75672593chr1:47834140ENST000004508080533_630180.0RegionNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST0000037187306133_14357.0229.0RegionLID
TgeneCMPK1chr11:75672593chr1:47834141ENST0000045080805133_1430180.0RegionLID
TgeneCMPK1chr11:75672593chr1:47834141ENST000004508080533_630180.0RegionNMP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneUVRAGchr11:75672593chr1:47834140ENST00000356136+715224_305233.0700.0Coiled coilOntology_term=ECO:0000255
HgeneUVRAGchr11:75672593chr1:47834141ENST00000356136+715224_305233.0700.0Coiled coilOntology_term=ECO:0000255
TgeneCMPK1chr11:75672593chr1:47834140ENST000003718730613_1857.0229.0Nucleotide bindingATP
TgeneCMPK1chr11:75672593chr1:47834141ENST000003718730613_1857.0229.0Nucleotide bindingATP
TgeneCMPK1chr11:75672593chr1:47834140ENST000003718730633_6357.0229.0RegionNMP
TgeneCMPK1chr11:75672593chr1:47834141ENST000003718730633_6357.0229.0RegionNMP


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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
UVRAG
CMPK1


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


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Related Drugs to UVRAG-CMPK1


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 UVRAG-CMPK1


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