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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:APRT-APRT (FusionGDB2 ID:5816)

Fusion Gene Summary for APRT-APRT

check button Fusion gene summary
Fusion gene informationFusion gene name: APRT-APRT
Fusion gene ID: 5816
HgeneTgene
Gene symbol

APRT

APRT

Gene ID

353

353

Gene nameadenine phosphoribosyltransferaseadenine phosphoribosyltransferase
SynonymsAMP|APRTDAMP|APRTD
Cytomap

16q24.3

16q24.3

Type of geneprotein-codingprotein-coding
Descriptionadenine phosphoribosyltransferaseAMP diphosphorylaseAMP pyrophosphorylasetransphosphoribosidaseadenine phosphoribosyltransferaseAMP diphosphorylaseAMP pyrophosphorylasetransphosphoribosidase
Modification date2020032220200322
UniProtAcc.

P07741

Ensembl transtripts involved in fusion geneENST00000378364, ENST00000426324, 
ENST00000563655, 
ENST00000378364, 
ENST00000426324, ENST00000563655, 
Fusion gene scores* DoF score2 X 2 X 1=46 X 10 X 4=240
# samples 28
** MAII scorelog2(2/4*10)=2.32192809488736log2(8/240*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: APRT [Title/Abstract] AND APRT [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAPRT(88876939)-APRT(88876876), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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

check buttonFusion gene breakpoints across APRT (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across APRT (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChiTaRS5.0N/ABG475137APRTchr16

88876939

+APRTchr16

88876876

-


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Fusion Gene ORF analysis for APRT-APRT

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000378364ENST00000378364APRTchr16

88876939

+APRTchr16

88876876

-
intron-3CDSENST00000378364ENST00000426324APRTchr16

88876939

+APRTchr16

88876876

-
intron-intronENST00000378364ENST00000563655APRTchr16

88876939

+APRTchr16

88876876

-
intron-3CDSENST00000426324ENST00000378364APRTchr16

88876939

+APRTchr16

88876876

-
intron-3CDSENST00000426324ENST00000426324APRTchr16

88876939

+APRTchr16

88876876

-
intron-intronENST00000426324ENST00000563655APRTchr16

88876939

+APRTchr16

88876876

-
intron-3CDSENST00000563655ENST00000378364APRTchr16

88876939

+APRTchr16

88876876

-
intron-3CDSENST00000563655ENST00000426324APRTchr16

88876939

+APRTchr16

88876876

-
intron-intronENST00000563655ENST00000563655APRTchr16

88876939

+APRTchr16

88876876

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for APRT-APRT


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for APRT-APRT


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

P07741

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 a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis.

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for APRT-APRT


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for APRT-APRT


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for APRT-APRT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneAPRTP07741DB016325-O-phosphono-alpha-D-ribofuranosyl diphosphateSmall moleculeApproved|Experimental|Investigational
TgeneAPRTP07741DB00173AdenineSmall moleculeApproved|Nutraceutical
TgeneAPRTP07741DB04272Citric acidSmall moleculeApproved|Nutraceutical|Vet_approved

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Related Diseases for APRT-APRT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAPRTC0268120Adenine phosphoribosyltransferase deficiency11CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneAPRTC0011570Mental Depression5PSYGENET
HgeneAPRTC0011581Depressive disorder5PSYGENET
HgeneAPRTC0451641Urolithiasis2CTD_human
HgeneAPRTC0006142Malignant neoplasm of breast1CTD_human
HgeneAPRTC0007134Renal Cell Carcinoma1CTD_human
HgeneAPRTC0022661Kidney Failure, Chronic1GENOMICS_ENGLAND
HgeneAPRTC0027707Nephritis, Interstitial1GENOMICS_ENGLAND
HgeneAPRTC0041696Unipolar Depression1PSYGENET
HgeneAPRTC0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
HgeneAPRTC0678222Breast Carcinoma1CTD_human
HgeneAPRTC1257931Mammary Neoplasms, Human1CTD_human
HgeneAPRTC1266042Chromophobe Renal Cell Carcinoma1CTD_human
HgeneAPRTC1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
HgeneAPRTC1266044Collecting Duct Carcinoma of the Kidney1CTD_human
HgeneAPRTC1269683Major Depressive Disorder1PSYGENET
HgeneAPRTC1306837Papillary Renal Cell Carcinoma1CTD_human
HgeneAPRTC1458155Mammary Neoplasms1CTD_human
HgeneAPRTC1561643Chronic Kidney Diseases1GENOMICS_ENGLAND
HgeneAPRTC36653822,8-Dihydroxyadenine Urolithiasis1CTD_human;ORPHANET
HgeneAPRTC4704874Mammary Carcinoma, Human1CTD_human
TgeneAPRTC0268120Adenine phosphoribosyltransferase deficiency11CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneAPRTC0011570Mental Depression5PSYGENET
TgeneAPRTC0011581Depressive disorder5PSYGENET
TgeneAPRTC0451641Urolithiasis2CTD_human
TgeneAPRTC0006142Malignant neoplasm of breast1CTD_human
TgeneAPRTC0007134Renal Cell Carcinoma1CTD_human
TgeneAPRTC0022661Kidney Failure, Chronic1GENOMICS_ENGLAND
TgeneAPRTC0027707Nephritis, Interstitial1GENOMICS_ENGLAND
TgeneAPRTC0041696Unipolar Depression1PSYGENET
TgeneAPRTC0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
TgeneAPRTC0678222Breast Carcinoma1CTD_human
TgeneAPRTC1257931Mammary Neoplasms, Human1CTD_human
TgeneAPRTC1266042Chromophobe Renal Cell Carcinoma1CTD_human
TgeneAPRTC1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
TgeneAPRTC1266044Collecting Duct Carcinoma of the Kidney1CTD_human
TgeneAPRTC1269683Major Depressive Disorder1PSYGENET
TgeneAPRTC1306837Papillary Renal Cell Carcinoma1CTD_human
TgeneAPRTC1458155Mammary Neoplasms1CTD_human
TgeneAPRTC1561643Chronic Kidney Diseases1GENOMICS_ENGLAND
TgeneAPRTC36653822,8-Dihydroxyadenine Urolithiasis1CTD_human;ORPHANET
TgeneAPRTC4704874Mammary Carcinoma, Human1CTD_human