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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:GPD2-SORD (FusionGDB2 ID:HG2820TG6652)

Fusion Gene Summary for GPD2-SORD

check button Fusion gene summary
Fusion gene informationFusion gene name: GPD2-SORD
Fusion gene ID: hg2820tg6652
HgeneTgene
Gene symbol

GPD2

SORD

Gene ID

2820

6652

Gene nameglycerol-3-phosphate dehydrogenase 2sorbitol dehydrogenase
SynonymsGDH2|GPDM|mGPDHHEL-S-95n|RDH|SDH|SORD1|XDH
Cytomap('GPD2')('SORD')

2q24.1

15q21.1

Type of geneprotein-codingprotein-coding
Descriptionglycerol-3-phosphate dehydrogenase, mitochondrialGPD-MGPDH-Mglycerol-3-phosphate dehydrogenase 2 (mitochondrial)mitochondrial glycerophosphate dehydrogenasemtGPDtesticular tissue protein Li 76sorbitol dehydrogenase(R,R)-butanediol dehydrogenaseL-iditol 2-dehydrogenaseepididymis secretory sperm binding protein Li 95npolyol dehydrogenaseribitol dehydrogenasexylitol dehydrogenase
Modification date2020031320200313
UniProtAcc

P43304

.
Ensembl transtripts involved in fusion geneENST00000310454, ENST00000409125, 
ENST00000409674, ENST00000438166, 
ENST00000496190, ENST00000540309, 
Fusion gene scores* DoF score6 X 6 X 4=1448 X 7 X 3=168
# samples 78
** MAII scorelog2(7/144*10)=-1.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GPD2 [Title/Abstract] AND SORD [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGPD2(157360417)-SORD(45366811), # 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
TgeneSORD

GO:0006062

sorbitol catabolic process

3365415|6870831|8487505|12962626

TgeneSORD

GO:0046370

fructose biosynthetic process

3365415|6870831|8487505

TgeneSORD

GO:0051160

L-xylitol catabolic process

8487505

TgeneSORD

GO:0051164

L-xylitol metabolic process

3365415



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/AFN115552GPD2chr2

157360417

-SORDchr15

45366811

-


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Fusion Gene ORF analysis for GPD2-SORD

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-3UTRENST00000310454ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-3UTRENST00000409125ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-3UTRENST00000409674ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-3UTRENST00000438166ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-3UTRENST00000496190ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-3UTRENST00000540309ENST00000267814GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000310454ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000310454ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000409125ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000409125ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000409674ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000409674ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000438166ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000438166ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000496190ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000496190ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000540309ENST00000558580GPD2chr2

157360417

-SORDchr15

45366811

-
intron-intronENST00000540309ENST00000559562GPD2chr2

157360417

-SORDchr15

45366811

-

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 GPD2-SORD


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)


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Fusion Protein Features for GPD2-SORD


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/:157360417/:45366811)
- 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
GPD2

P43304

.
FUNCTION: Calcium-responsive mitochondrial glycerol-3-phosphate dehydrogenase which seems to be a key component of the pancreatic beta-cell glucose-sensing device. {ECO:0000269|PubMed:9070847}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 GPD2-SORD


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 GPD2-SORD


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 GPD2-SORD


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for GPD2-SORD


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGPD2C0001787Osteoporosis, Age-Related1CTD_human
HgeneGPD2C0002152Alloxan Diabetes1CTD_human
HgeneGPD2C0011853Diabetes Mellitus, Experimental1CTD_human
HgeneGPD2C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneGPD2C0029456Osteoporosis1CTD_human
HgeneGPD2C0029459Osteoporosis, Senile1CTD_human
HgeneGPD2C0038433Streptozotocin Diabetes1CTD_human
HgeneGPD2C0268583Methylmalonic acidemia1CTD_human
HgeneGPD2C0751406Post-Traumatic Osteoporosis1CTD_human
HgeneGPD2C1855119Methylmalonic aciduria1CTD_human
TgeneC0019193Hepatitis, Toxic1CTD_human
TgeneC0027055Myocardial Reperfusion Injury1CTD_human
TgeneC0520459Necrotizing Enterocolitis1CTD_human
TgeneC0860207Drug-Induced Liver Disease1CTD_human
TgeneC1262760Hepatitis, Drug-Induced1CTD_human
TgeneC3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneC4279912Chemically-Induced Liver Toxicity1CTD_human