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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:GRID1-GLUD1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GRID1-GLUD1
FusionPDB ID: 34744
FusionGDB2.0 ID: 34744
HgeneTgene
Gene symbol

GRID1

GLUD1

Gene ID

2894

2746

Gene nameglutamate ionotropic receptor delta type subunit 1glutamate dehydrogenase 1
SynonymsGluD1GDH|GDH1|GLUD
Cytomap

10q23.1-q23.2

10q23.2

Type of geneprotein-codingprotein-coding
Descriptionglutamate receptor ionotropic, delta-1gluR delta-1 subunitglutamate receptor delta-1 subunitglutamate dehydrogenase 1, mitochondrialepididymis secretory sperm binding proteinepididymis tissue sperm binding protein Li 18mPglutamate dehydrogenase (NAD(P)+)
Modification date2020031320200329
UniProtAcc

Q9ULK0

P00367

Ensembl transtripts involved in fusion geneENST idsENST00000327946, ENST00000536331, 
ENST00000552278, 
ENST00000537649, 
ENST00000544149, ENST00000465164, 
ENST00000277865, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 8 X 6=48010 X 7 X 8=560
# samples 1111
** MAII scorelog2(11/480*10)=-2.12553088208386
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/560*10)=-2.34792330342031
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: GRID1 [Title/Abstract] AND GLUD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GRID1(88123698)-GLUD1(88836413), # samples:3
Anticipated loss of major functional domain due to fusion event.GRID1-GLUD1 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.
GRID1-GLUD1 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
TgeneGLUD1

GO:0006537

glutamate biosynthetic process

11032875

TgeneGLUD1

GO:0006538

glutamate catabolic process

6121377|11032875


check buttonFusion gene breakpoints across GRID1 (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 GLUD1 (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
ChimerDB4BLCATCGA-K4-A6MB-01AGRID1chr10

88123698

-GLUD1chr10

88836413

-
ChimerDB4BLCATCGA-K4-A6MBGRID1chr10

88123697

-GLUD1chr10

88836413

-


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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)
ENST00000327946GRID1chr1088123698-ENST00000277865GLUD1chr1088836413-2818321861552488
ENST00000327946GRID1chr1088123697-ENST00000277865GLUD1chr1088836413-2818321861552488

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
ENST00000327946ENST00000277865GRID1chr1088123698-GLUD1chr1088836413-0.0003395720.9996604
ENST00000327946ENST00000277865GRID1chr1088123697-GLUD1chr1088836413-0.0003395720.9996604

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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

>34744_34744_1_GRID1-GLUD1_GRID1_chr10_88123697_ENST00000327946_GLUD1_chr10_88836413_ENST00000277865_length(amino acids)=488AA_BP=78
MEALTLWLLPWICQCVSVRADSIIHIGAIFEENAAKDDRVFQLAVSDLSLNDDILQSEKITYSIKVIEANNPFQAVQEGIRYSTDVSVDE
VKALASLMTYKCAVVDVPFGGAKAGVKINPKNYTDNELEKITRRFTMELAKKGFIGPGIDVPAPDMSTGEREMSWIADTYASTIGHYDIN
AHACVTGKPISQGGIHGRISATGRGVFHGIENFINEASYMSILGMTPGFGDKTFVVQGFGNVGLHSMRYLHRFGAKCIAVGESDGSIWNP
DGIDPKELEDFKLQHGSILGFPKAKPYEGSILEADCDILIPAASEKQLTKSNAPRVKAKIIAEGANGPTTPEADKIFLERNIMVIPDLYL
NAGGVTVSYFEWLKNLNHVSYGRLTFKYERDSNYHLLMSVQESLERKFGKHGGTIPIVPTAEFQDRISGASEKDIVHSGLAYTMERSARQ

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

>34744_34744_2_GRID1-GLUD1_GRID1_chr10_88123698_ENST00000327946_GLUD1_chr10_88836413_ENST00000277865_length(amino acids)=488AA_BP=78
MEALTLWLLPWICQCVSVRADSIIHIGAIFEENAAKDDRVFQLAVSDLSLNDDILQSEKITYSIKVIEANNPFQAVQEGIRYSTDVSVDE
VKALASLMTYKCAVVDVPFGGAKAGVKINPKNYTDNELEKITRRFTMELAKKGFIGPGIDVPAPDMSTGEREMSWIADTYASTIGHYDIN
AHACVTGKPISQGGIHGRISATGRGVFHGIENFINEASYMSILGMTPGFGDKTFVVQGFGNVGLHSMRYLHRFGAKCIAVGESDGSIWNP
DGIDPKELEDFKLQHGSILGFPKAKPYEGSILEADCDILIPAASEKQLTKSNAPRVKAKIIAEGANGPTTPEADKIFLERNIMVIPDLYL
NAGGVTVSYFEWLKNLNHVSYGRLTFKYERDSNYHLLMSVQESLERKFGKHGGTIPIVPTAEFQDRISGASEKDIVHSGLAYTMERSARQ

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

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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/chr10:88123698/chr10:88836413)
- 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
GRID1

Q9ULK0

GLUD1

P00367

FUNCTION: Receptor for glutamate. L-glutamate acts as an excitatory neurotransmitter at many synapses in the central nervous system. The postsynaptic actions of Glu are mediated by a variety of receptors that are named according to their selective agonists.FUNCTION: Mitochondrial glutamate dehydrogenase that catalyzes the conversion of L-glutamate into alpha-ketoglutarate. Plays a key role in glutamine anaplerosis by producing alpha-ketoglutarate, an important intermediate in the tricarboxylic acid cycle (PubMed:11032875, PubMed:16959573, PubMed:11254391, PubMed:16023112). Plays a role in insulin homeostasis (PubMed:9571255, PubMed:11297618). May be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate (By similarity). {ECO:0000250|UniProtKB:P10860, ECO:0000269|PubMed:11032875, ECO:0000269|PubMed:11254391, ECO:0000269|PubMed:11297618, ECO:0000269|PubMed:16023112, ECO:0000269|PubMed:16959573, ECO:0000269|PubMed:9571255}.

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

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-21621_56278.333333333333331010.0Topological domainExtracellular
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216584_63778.333333333333331010.0Topological domainCytoplasmic
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216659_83078.333333333333331010.0Topological domainExtracellular
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216852_100978.333333333333331010.0Topological domainCytoplasmic
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-21621_56278.333333333333331010.0Topological domainExtracellular
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216584_63778.333333333333331010.0Topological domainCytoplasmic
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216659_83078.333333333333331010.0Topological domainExtracellular
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216852_100978.333333333333331010.0Topological domainCytoplasmic
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216563_58378.333333333333331010.0TransmembraneHelical
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216638_65878.333333333333331010.0TransmembraneHelical
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-216831_85178.333333333333331010.0TransmembraneHelical
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216563_58378.333333333333331010.0TransmembraneHelical
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216638_65878.333333333333331010.0TransmembraneHelical
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-216831_85178.333333333333331010.0TransmembraneHelical
TgeneGLUD1chr10:88123697chr10:88836413ENST00000277865013141_143148.33333333333334559.0Nucleotide bindingNAD
TgeneGLUD1chr10:88123698chr10:88836413ENST00000277865013141_143148.33333333333334559.0Nucleotide bindingNAD


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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
GRID1
GLUD1


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
HgeneGRID1chr10:88123697chr10:88836413ENST00000327946-21621_43678.333333333333331010.0CBLN1
HgeneGRID1chr10:88123698chr10:88836413ENST00000327946-21621_43678.333333333333331010.0CBLN1


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Related Drugs to GRID1-GLUD1


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 GRID1-GLUD1


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