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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:HOMER1-DMGDH (FusionGDB2 ID:37347)

Fusion Gene Summary for HOMER1-DMGDH

check button Fusion gene summary
Fusion gene informationFusion gene name: HOMER1-DMGDH
Fusion gene ID: 37347
HgeneTgene
Gene symbol

HOMER1

DMGDH

Gene ID

9456

29958

Gene namehomer scaffold protein 1dimethylglycine dehydrogenase
SynonymsHOMER|HOMER1A|HOMER1B|HOMER1C|SYN47|Ves-1DMGDHD|ME2GLYDH
Cytomap

5q14.1

5q14.1

Type of geneprotein-codingprotein-coding
Descriptionhomer protein homolog 1homer homolog 1homer scaffolding protein 1homer, neuronal immediate early gene, 1homer-1dimethylglycine dehydrogenase, mitochondrial
Modification date2020031320200313
UniProtAcc

Q86YM7

Q9UI17

Ensembl transtripts involved in fusion geneENST00000334082, ENST00000508576, 
ENST00000282260, ENST00000535690, 
ENST00000380311, ENST00000540686, 
ENST00000255189, ENST00000520388, 
Fusion gene scores* DoF score7 X 6 X 5=2102 X 3 X 2=12
# samples 83
** MAII scorelog2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HOMER1 [Title/Abstract] AND DMGDH [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHOMER1(78734833)-DMGDH(78359610), # samples:2
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
HgeneHOMER1

GO:0051592

response to calcium ion

14505576


check buttonFusion gene breakpoints across HOMER1 (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 DMGDH (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
ChimerDB4LUSCTCGA-56-7223-01AHOMER1chr5

78734833

-DMGDHchr5

78359610

-
ChimerDB4LUSCTCGA-56-7223HOMER1chr5

78734833

-DMGDHchr5

78329231

-
ChimerDB4LUSCTCGA-56-7223HOMER1chr5

78734833

-DMGDHchr5

78359610

-


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Fusion Gene ORF analysis for HOMER1-DMGDH

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
5CDS-5UTRENST00000334082ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-5UTRENST00000334082ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-5UTRENST00000508576ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-5UTRENST00000508576ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-intronENST00000334082ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-intronENST00000334082ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000334082ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000334082ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-intronENST00000334082ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000334082ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000508576ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-intronENST00000508576ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000508576ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000508576ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78359610

-
5CDS-intronENST00000508576ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78329231

-
5CDS-intronENST00000508576ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-5UTRENST00000282260ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-5UTRENST00000282260ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-5UTRENST00000535690ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-5UTRENST00000535690ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-intronENST00000282260ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-intronENST00000282260ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000282260ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000282260ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-intronENST00000282260ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000282260ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000535690ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-intronENST00000535690ENST00000255189HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000535690ENST00000380311HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000535690ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78359610

-
intron-intronENST00000535690ENST00000520388HOMER1chr5

78734833

-DMGDHchr5

78329231

-
intron-intronENST00000535690ENST00000540686HOMER1chr5

78734833

-DMGDHchr5

78329231

-

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 HOMER1-DMGDH


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.
genomic feature

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 HOMER1-DMGDH


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/:78734833/:78359610)
- 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
HOMER1

Q86YM7

DMGDH

Q9UI17

FUNCTION: Postsynaptic density scaffolding protein. Binds and cross-links cytoplasmic regions of GRM1, GRM5, ITPR1, DNM3, RYR1, RYR2, SHANK1 and SHANK3. By physically linking GRM1 and GRM5 with ER-associated ITPR1 receptors, it aids the coupling of surface receptors to intracellular calcium release. May also couple GRM1 to PI3 kinase through its interaction with AGAP2. Isoform 1 regulates the trafficking and surface expression of GRM5. Isoform 3 acts as a natural dominant negative, in dynamic competition with constitutively expressed isoform 1 to regulate synaptic metabotropic glutamate function. Isoform 3, may be involved in the structural changes that occur at synapses during long-lasting neuronal plasticity and development. Forms a high-order complex with SHANK1, which in turn is necessary for the structural and functional integrity of dendritic spines (By similarity). Negatively regulates T cell activation by inhibiting the calcineurin-NFAT pathway. Acts by competing with calcineurin/PPP3CA for NFAT protein binding, hence preventing NFAT activation by PPP3CA (PubMed:18218901). {ECO:0000250|UniProtKB:Q9Z214, ECO:0000269|PubMed:18218901}.FUNCTION: Catalyzes the demethylation of N,N-dimethylglycine to sarcosine. Also has activity with sarcosine in vitro. {ECO:0000269|PubMed:27486859}.

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 HOMER1-DMGDH


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 HOMER1-DMGDH


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 HOMER1-DMGDH


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 HOMER1-DMGDH


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource