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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:SLC22A23-ECHDC1 (FusionGDB2 ID:HG63027TG55862)

Fusion Gene Summary for SLC22A23-ECHDC1

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC22A23-ECHDC1
Fusion gene ID: hg63027tg55862
HgeneTgene
Gene symbol

SLC22A23

ECHDC1

Gene ID

63027

55862

Gene namesolute carrier family 22 member 23ethylmalonyl-CoA decarboxylase 1
SynonymsC6orf85HEL-S-76|MMCD|dJ351K20.2
Cytomap('SLC22A23')('ECHDC1')

6p25.2

6q22.33

Type of geneprotein-codingprotein-coding
Descriptionsolute carrier family 22 member 23ion transporter proteinethylmalonyl-CoA decarboxylaseenoyl CoA hydratase domain containing 1enoyl Coenzyme A hydratase domain containing 1enoyl-CoA hydratase domain-containing protein 1epididymis secretory protein Li 76methylmalonyl-CoA decarboxylase
Modification date2020031320200313
UniProtAcc.

Q9NTX5

Ensembl transtripts involved in fusion geneENST00000380302, ENST00000406686, 
ENST00000436008, ENST00000490273, 
ENST00000380298, ENST00000433689, 
Fusion gene scores* DoF score12 X 5 X 9=5408 X 7 X 6=336
# samples 1411
** MAII scorelog2(14/540*10)=-1.94753258010586
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/336*10)=-1.6109577092541
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLC22A23 [Title/Abstract] AND ECHDC1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLC22A23(3324068)-ECHDC1(127652175), # samples:3
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 button Fusion gene information
* 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-HQ-A2OE-01ASLC22A23chr6

3324068

-ECHDC1chr6

127652175

-


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Fusion Gene ORF analysis for SLC22A23-ECHDC1

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-5UTRENST00000380302ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000380302ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000406686ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000436008ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-5UTRENST00000490273ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000380302ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000380302ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000380302ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000406686ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000406686ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000406686ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000436008ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000436008ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000436008ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000490273ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000490273ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
5CDS-intronENST00000490273ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000380298ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000309620SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000368289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000368291SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000430841SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000454859SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000474289SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-5UTRENST00000433689ENST00000531967SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000380298ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000380298ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000380298ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000433689ENST00000454591SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000433689ENST00000488087SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-
intron-intronENST00000433689ENST00000528402SLC22A23chr6

3324068

-ECHDC1chr6

127652175

-

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 SLC22A23-ECHDC1


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 SLC22A23-ECHDC1


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/:3324068/:127652175)
- 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
.ECHDC1

Q9NTX5

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}.FUNCTION: Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading (PubMed:22016388). Also has methylmalonyl-CoA decarboxylase activity at lower level (By similarity). {ECO:0000250|UniProtKB:Q9D9V3, ECO:0000269|PubMed:22016388}.

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 SLC22A23-ECHDC1


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 SLC22A23-ECHDC1


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 SLC22A23-ECHDC1


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 SLC22A23-ECHDC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLC22A23C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0019193Hepatitis, Toxic1CTD_human
TgeneC0025202melanoma1CTD_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